/usr/include/ncbi/subutil.h is in libncbi6-dev 6.1.20120620-8.
This file is owned by root:root, with mode 0o644.
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1822 1823 1824 1825 1826 1827 1828 | /* subutil.h
* >> Set tabs to 4 spaces for a nice printout
*
* ===========================================================================
*
* PUBLIC DOMAIN NOTICE
* National Center for Biotechnology Information
*
* This software/database is a "United States Government Work" under the
* terms of the United States Copyright Act. It was written as part of
* the author's official duties as a United States Government employee and
* thus cannot be copyrighted. This software/database is freely available
* to the public for use. The National Library of Medicine and the U.S.
* Government have not placed any restriction on its use or reproduction.
*
* Although all reasonable efforts have been taken to ensure the accuracy
* and reliability of the software and data, the NLM and the U.S.
* Government do not and cannot warrant the performance or results that
* may be obtained by using this software or data. The NLM and the U.S.
* Government disclaim all warranties, express or implied, including
* warranties of performance, merchantability or fitness for any particular
* purpose.
*
* Please cite the author in any work or product based on this material.
*
* ===========================================================================
*
* File Name: subutil.h
*
* Author: James Ostell
*
* Version Creation Date: 11/3/93
*
* $Revision: 6.88 $
*
* File Description: Utilities for creating ASN.1 submissions
*
* Modifications:
* --------------------------------------------------------------------------
* Date Name Description of modification
* ------- ---------- -----------------------------------------------------
*
* ==========================================================================
*/
#ifndef _NCBI_SubUtil_
#define _NCBI_SubUtil_
#ifndef _NCBI_Submit_
#include <objsub.h>
#endif
#undef NLM_EXTERN
#ifdef NLM_IMPORT
#define NLM_EXTERN NLM_IMPORT
#else
#define NLM_EXTERN extern
#endif
#ifdef __cplusplus
extern "C" {
#endif
/*****************************************************************************
*
* Create a GenBank direct submission
* This supports a basic set of datatypes for making a new direct
* submission to GenBank in ASN.1. It is designed for folks wanting to
* read their own data storage format, then make a valid direct submission
* without going through an intermediate tool.
*
* You may have many "entries" in a single submission. A single entry
* may contain:
* One protein sequence (called a "Bioseq")
* One nucleic acid sequence (called a "Bioseq")
* One nucleic acid sequence for which you only have a series of
* sequence pieces (e.g. you sequenced around the exons of a
* genomic sequence, but not the introns) (called a "segmented
* set")
* One nucleic acid sequence and the protein sequences it codes for.
* (nucleic acid may a a single Bioseq or a segmented set)
* (this entry called a "nuc-prot set")
*
* NCBI considers the protein sequences part
* of the submission, and they are created as proteins in their own right
* by the routines below. You can either supply the protein sequence from
* your own software (best case), in which we check that the coding region
* you supply translates to it. If you do not supply a protein sequence,
* then all we can do is check that it translates without stops.
*
* NCBI also considers "gene" to refer to a region of nucleic acid
* within which are found elements (such as promoters, coding regions,etc)
* leading to a phenomenon recognized as a gene (note this also accomodates
* anonymous markers as well as expressed products). This is in contrast to
* so other notions that a gene is simply a qualifier on other features of
* the DNA. A separate function to produce a gene feature is supplied. The
* intervals given for it should include the intervals for the other
* features it contains.
*
* The process of building the direct submission is roughly:
*
* Create the submission
* Add the submission citation
* Create an entry (can be 1 or more sequences)
* Add the organism information
* Add any publication citations
* Add the sequences
* Fill in the residues
* Add the features
* Validate the entry
* Write the entry
* Free the memory used
*
* Each element may have subfunctions:
*
* Create a citation
* Add author names
* Add author affiliation
*
* Create a sequence
* Add modifiers
*
* Create a feature
* Add information specific to type of feature
* Add intervals on the sequence
*
*****************************************************************************/
typedef Boolean (* SubErrorFunc) (CharPtr msg);
typedef struct ncbisub {
SeqSubmitPtr ssp; /* the submission */
SubErrorFunc err_func; /* the error handler */
Int2 gap_count; /* for unique gap names in segs */
CharPtr submittor_key; /* used for turning local SeqId to General */
} NCBISub, PNTR NCBISubPtr;
#define PubPtr ValNodePtr /* should really be typedeffed */
/*****************************************************************************
*
* Prototypes for building a direct submission
*
*****************************************************************************/
/* default error handler */
NLM_EXTERN Boolean DefaultSubErrorFunc (CharPtr msg);
/*****************************************************************************
*
* Create/Free the NCBISub
*
*****************************************************************************/
NLM_EXTERN NCBISubPtr NCBISubCreate (
CharPtr last_name,
CharPtr first_name,
CharPtr middle_name,
CharPtr initials, /* separated by periods, no initial for last name */
CharPtr suffix, /* Jr. Sr. III */
CharPtr affil, /* e.g. "Xyz University" */
CharPtr div, /* e.g. "Dept of Biology" */
CharPtr street, /* e.g. "123 Academic Road" */
CharPtr city, /* e.g. "Metropolis" */
CharPtr sub, /* e.g. "Massachusetts" */
CharPtr country , /* e.g. "USA" */
CharPtr postal_code, /* e.g."02133" */
CharPtr phone ,
CharPtr fax ,
CharPtr email,
Boolean hold_until_publish ,
Int2 release_month ,
Int2 release_day ,
Int2 release_year );
NLM_EXTERN Boolean DefineSubmittorKey(
NCBISubPtr nsp,
CharPtr submittor_key ); /* submitting large scale lab, for regular submissions */
/**** WARNING: NCBISubBuild() is the old style submission ***/
/**** It has been replaced by NCBISubCreate() ***/
/**** NCBISubBuild will be discontinued ***/
NLM_EXTERN NCBISubPtr NCBISubBuild (
CharPtr name,
CharPtr PNTR address ,
CharPtr phone ,
CharPtr fax ,
CharPtr email,
Boolean hold_until_publish ,
Int2 release_month,
Int2 release_day,
Int2 release_year );
/** every submission must have 1 submission citation **/
/** see below to add authors and affiliation **********/
NLM_EXTERN Boolean CitSubForSubmission (
NCBISubPtr submission,
PubPtr cit_sub );
NLM_EXTERN Boolean AddToolToSub (
NCBISubPtr nsp,
CharPtr tool );
NLM_EXTERN Boolean AddCommentToSub (
NCBISubPtr nsp,
CharPtr comment );
NLM_EXTERN Boolean AddTypeToSub (
NCBISubPtr nsp,
Uint1 type );
NLM_EXTERN Boolean NCBISubWrite (
NCBISubPtr ssp,
CharPtr filename );
NLM_EXTERN NCBISubPtr NCBISubFree (
NCBISubPtr ssp );
/*****************************************************************************
*
* You can (should) run the ncbi validator routines on your final submission.
* It returns a count of all errors or questions found.
*
* The errfile parameter is no longer supported. Errors are directed
* based on the ErrLog functions in the toolkit. If you have done none
* of this, then errors will appear on stderr.
*
*****************************************************************************/
NLM_EXTERN Int2 NCBISubValidate (NCBISubPtr nsp, FILE * errfile);
/*****************************************************************************
*
* Add Entries to the Submission
* Add Sequences to the Entries
*
*****************************************************************************/
/*****************************************************************************
*
* About Sequence Identifiers:
*
* Note that in all functions below where you create a Bioseq in your entry,
* you can supply a number of different pieces of information to make a
* sequence id.
*
* local_name: This is a string for whatever name you call this sequence
* locally. Could be a clone name or whatever. There are no
* limits on this other than it should be unique in the
* submission. It is REQUIRED.
*
* SeqEntryPtr: Returned by the function, this is a pointer to the Bioseq.
*
* In later functions, such as adding feature locations, you can refer to
* the Bioseq you created either with the local_name or directly with the
* SeqEntryPtr. Whatever is more convenient for you is fine.
*
* The other ids only apply to updates. These allow you to update your
* entry in GenBank simply by sending a new entry with the same accession
* number you were issued on the last one. In this case you should also
* be sure to add the create_date, which will be returned to you in the
* ASN.1 of your direct submission after processing. This is not absolutely
* required, but does let us check that it is the right entry (errors
* could occur when you enter your old accession number).
*
* genbank_locus: OPTIONAL on update. The name appearing on the LOCUS line.
* genbank_accession: REQUIRED on update.
* gi_number: OPTIONAL on update for now. The unique ID assigned by NCBI
* to a particular sequence (DNA or protein) in your entry.
*
* If you update your entry, whether you change the sequence or not, the
* accession number and locus will remain the same, so people can retrieve
* your new data with the old id. However, the gi_number is explicitly keyed
* to the sequence, and will change if there are any changes/additions to
* the sequence. In addition, a history will be created indicating the old
* gi_number and the date the new entry replaced it. Both old and new
* entries will be available from NCBI for retrieval on gi_number. Only the
* new entry will appear in the next GenBank or Entrez release.
*
*****************************************************************************/
/*** Entry contains only 1 raw Bioseq ***/
NLM_EXTERN SeqEntryPtr AddSeqOnlyToSubmission (
NCBISubPtr submission ,
CharPtr local_name ,
CharPtr genbank_locus ,
CharPtr genbank_accession ,
Int4 gi_number ,
Int2 molecule_class,
Int2 molecule_type ,
Int4 length ,
Int2 topology ,
Int2 strandedness );
/*** Entry contains a segmented set of Bioseqs ***/
NLM_EXTERN SeqEntryPtr AddSegmentedSeqToSubmission (
NCBISubPtr submission ,
CharPtr local_name ,
CharPtr genbank_locus ,
CharPtr genbank_accession ,
Int4 gi_number ,
Int2 molecule_class,
Int2 molecule_type ,
Int4 length ,
Int2 topology ,
Int2 strandedness );
NLM_EXTERN SeqEntryPtr AddSeqToSegmentedEntry (
NCBISubPtr submission,
SeqEntryPtr segmented_seq_entry,
CharPtr local_name ,
CharPtr genbank_locus ,
CharPtr genbank_accession ,
Int4 gi_number ,
Int2 molecule_class,
Int2 molecule_type ,
Int4 length ,
Int2 topology ,
Int2 strandedness );
NLM_EXTERN Boolean AddGapToSegmentedEntry (
NCBISubPtr submission,
SeqEntryPtr segmented_seq_entry,
Int4 length_of_gap ); /** 0 if not known */
NLM_EXTERN Boolean AddReferenceToSegmentedEntry (
NCBISubPtr submission ,
SeqEntryPtr segmented_seq_entry,
CharPtr genbank_accession ,
Int4 gi_number ,
Int4 from ,
Int4 to ,
Boolean on_plus_strand );
/*** Entry contains sets of similar sequences ***/
NLM_EXTERN SeqEntryPtr AddPopSetToSubmission (
NCBISubPtr submission );
NLM_EXTERN SeqEntryPtr AddPhySetToSubmission (
NCBISubPtr submission );
NLM_EXTERN SeqEntryPtr AddMutSetToSubmission (
NCBISubPtr submission );
NLM_EXTERN SeqEntryPtr AddGenBankSetToSubmission (
NCBISubPtr submission );
/*** Entry contains nucleotide and translated proteins ***/
NLM_EXTERN SeqEntryPtr AddNucProtToSubmission (
NCBISubPtr submission );
NLM_EXTERN SeqEntryPtr AddSeqToNucProtEntry ( /** add unsegmented nuc or prot bioseq */
NCBISubPtr submission,
SeqEntryPtr nuc_prot_entry,
CharPtr local_name ,
CharPtr genbank_locus ,
CharPtr genbank_accession ,
Int4 gi_number ,
Int2 molecule_class,
Int2 molecule_type ,
Int4 length ,
Int2 topology ,
Int2 strandedness );
/** add segmented nuc or prot bioseq set */
NLM_EXTERN SeqEntryPtr AddSegmentedSeqToNucProtEntry (
NCBISubPtr submission,
SeqEntryPtr nuc_prot_entry ,
CharPtr local_name ,
CharPtr genbank_locus ,
CharPtr genbank_accession ,
Int4 gi_number ,
Int2 molecule_class,
Int2 molecule_type ,
Int4 length ,
Int2 topology ,
Int2 strandedness );
NLM_EXTERN SeqEntryPtr AddDeltaSeqToNucProtEntry (
NCBISubPtr submission,
SeqEntryPtr nuc_prot_entry ,
CharPtr local_name ,
CharPtr genbank_locus ,
CharPtr genbank_accession ,
Int4 gi_number ,
Int2 molecule_class,
Int2 molecule_type ,
Int4 length ,
Int2 topology ,
Int2 strandedness );
/**** Entry contains one delta sequence ****/
NLM_EXTERN SeqEntryPtr AddDeltaSeqOnlyToSubmission (
NCBISubPtr submission,
CharPtr local_name ,
CharPtr genbank_locus ,
CharPtr genbank_accession ,
Int4 gi_number ,
Int2 molecule_class,
Int2 molecule_type ,
Int4 length ,
Int2 topology ,
Int2 strandedness );
NLM_EXTERN Boolean AddGapToDeltaSeq (
NCBISubPtr submission,
SeqEntryPtr delta_seq_entry,
Int4 length_of_gap ); /** 0 if not known */
NLM_EXTERN SeqLitPtr AddFakeGapToDeltaSeq (
NCBISubPtr submission,
SeqEntryPtr delta_seq_entry,
Int4 length_of_gap ); /** returns slp so program can set lim - unk fuzz after empty gaps are spread */
NLM_EXTERN SeqLitPtr AddLiteralToDeltaSeq (
NCBISubPtr submission,
SeqEntryPtr delta_seq_entry,
Int4 length_of_sequence );
#define MOLECULE_CLASS_DNA 1
#define MOLECULE_CLASS_RNA 2
#define MOLECULE_CLASS_NUC 4
#define MOLECULE_CLASS_PROTEIN 3
#define MOLECULE_TYPE_GENOMIC 1
#define MOLECULE_TYPE_PRE_MRNA 2
#define MOLECULE_TYPE_MRNA 3
#define MOLECULE_TYPE_RRNA 4
#define MOLECULE_TYPE_TRNA 5
#define MOLECULE_TYPE_SNRNA 6
#define MOLECULE_TYPE_SCRNA 7
#define MOLECULE_TYPE_PEPTIDE 8
#define MOLECULE_TYPE_OTHER_GENETIC_MATERIAL 9
#define MOLECULE_TYPE_GENOMIC_MRNA_MIX 10
#define MOLECULE_TYPE_CRNA 11
#define MOLECULE_TYPE_SNORNA 12
#define MOLECULE_TYPE_TRANSCRIBED_RNA 13
#define MOLECULE_TYPE_NCRNA 14
#define MOLECULE_TYPE_TMRNA 15
#define TOPOLOGY_LINEAR 1
#define TOPOLOGY_CIRCULAR 2
#define TOPOLOGY_TANDEM 3
#define STRANDEDNESS_SINGLE 1
#define STRANDEDNESS_DOUBLE 2
/******************************************************************
*
* Fill in Bases or Amino Acids
* 1) You may call functions as often per bioseq as you like
* up to the length of the Bioseq
* 2) All codes are iupac and defined in /ncbi/data/seqcode.prt
* as an ASN.1 file used by this code. Excerpts at the
* end of this file. Even though it's ASN.1 you will find
* you can read it with no trouble.
* 3) IUPAC codes are UPPER CASE. These functions will upper
* case for you.
* 4) In nucleic acids 'U' will be changed to 'T'
* 5) In both cases, non-letters will be stripped from the
* the input strings to facilate input from external
* formatted files with numbers and internal spaces and
* such.
*
******************************************************************/
NLM_EXTERN Boolean AddBasesToBioseq (
NCBISubPtr submission ,
SeqEntryPtr the_seq ,
CharPtr the_bases );
NLM_EXTERN Boolean AddAminoAcidsToBioseq (
NCBISubPtr submission ,
SeqEntryPtr the_seq ,
CharPtr the_aas );
/** variant functions for Delta sequences ***/
NLM_EXTERN Boolean AddBasesToLiteral (
NCBISubPtr submission ,
SeqLitPtr the_literal ,
CharPtr the_bases );
NLM_EXTERN Boolean AddAminoAcidsToLiteral (
NCBISubPtr submission ,
SeqLitPtr the_literal ,
CharPtr the_aas );
/*****************************************************************************
*
* Add Annotations to Entries
*
*****************************************************************************/
NLM_EXTERN Boolean AddTitleToEntry (
NCBISubPtr submission,
SeqEntryPtr entry ,
CharPtr title );
NLM_EXTERN Boolean AddSecondaryAccnToEntry (
NCBISubPtr submission,
SeqEntryPtr entry ,
CharPtr accn );
/*****************************************************************
*
* rules for long comments
* 1) include no non-ascii characters (e.g. \t \r \n)
* 2) you may force a line feed on display by using tilde '~'
* 3) you format a table by adding leading spaces after a '~'
* 4) non-ascii chars will be converted on input (also for
* title) \n='~', all others='#'
*
*****************************************************************/
NLM_EXTERN Boolean AddCommentToEntry (
NCBISubPtr submission,
SeqEntryPtr entry ,
CharPtr comment );
NLM_EXTERN Boolean AddOrganismToEntryNew (
NCBISubPtr submission,
SeqEntryPtr entry ,
CharPtr scientific_name ,
CharPtr common_name ,
CharPtr virus_name ,
CharPtr strain ,
CharPtr synonym1,
CharPtr synonym2,
CharPtr synonym3,
CharPtr taxonomy );
/** AddOrganismToEntryNew() defaults to universal code (0)
** for both cytoplasmic and mitochondiral ribosomes. You
** also supply the code when you create a CdRegion. If the
** CdRegion code does not match the organism code, the
** validator will warn, but will translate by CdRegion code.
** if you need an alternate code, SetGeneticCodeForEntry()
** can be used to eliminate the conflict. See table of genetic
** codes at end of this file. You should call
** AddOrganismToEntryNew() before calling
** SetGeneticCodeForEntry() **/
NLM_EXTERN Boolean AddOrganismToEntryEx (
NCBISubPtr submission,
SeqEntryPtr entry ,
CharPtr scientific_name ,
CharPtr common_name ,
CharPtr virus_name ,
CharPtr strain ,
CharPtr synonym1,
CharPtr synonym2,
CharPtr synonym3,
CharPtr taxonomy,
Int4 taxid );
/** AddOrganismToEntryEx() allows taxonID to be entered **/
NLM_EXTERN Boolean SetGeneticCodeForEntry (
NCBISubPtr submission,
SeqEntryPtr entry,
Uint1 genetic_code, /* for cytoplasm */
Uint1 mito_code ); /* for mitochondria */
/**************************************************
* OBSOLETE!!! do not use. Use AddOrganismToEntryNew
*
**************************************************/
NLM_EXTERN Boolean AddOrganismToEntry (
NCBISubPtr submission,
SeqEntryPtr entry ,
CharPtr scientific_name ,
CharPtr common_name ,
CharPtr virus_name ,
CharPtr strain ,
CharPtr synonym1,
CharPtr synonym2,
CharPtr synonym3);
NLM_EXTERN Boolean AddGenBankBlockToEntry (
NCBISubPtr submission,
SeqEntryPtr entry ,
CharPtr taxonomy ,
CharPtr division ,
CharPtr keyword1 ,
CharPtr keyword2 ,
CharPtr keyword3 );
#define GENOME_unknown 0
#define GENOME_genomic 1
#define GENOME_chloroplast 2
#define GENOME_chromoplast 3
#define GENOME_kinetoplast 4
#define GENOME_mitochondrion 5
#define GENOME_plastid 6
#define GENOME_macronuclear 7
#define GENOME_extrachrom 8
#define GENOME_plasmid 9
#define GENOME_transposon 10
#define GENOME_insertion_seq 11
#define GENOME_cyanelle 12
#define GENOME_proviral 13
#define GENOME_virion 14
#define GENOME_nucleomorph 15
#define GENOME_apicoplast 16
#define GENOME_leucoplast 17
#define GENOME_proplastid 18
#define GENOME_endogenous_virus 19
#define GENOME_hydrogenosome 20
#define GENOME_chromosome 21
#define GENOME_chromatophore 22
/********************************************
* Genome describes the type of genome from which the DNA or gene for
* a protein is located. Values are:
genome INTEGER { -- biological context
unknown (0) ,
genomic (1) ,
chloroplast (2) ,
chromoplast (3) ,
kinetoplast (4) ,
mitochondrion (5) ,
plastid (6) ,
macronuclear (7) ,
extrachrom (8) ,
plasmid (9) ,
transposon (10) ,
insertion-seq (11) ,
cyanelle (12) ,
proviral (13) ,
virion (14) } DEFAULT unknown ,
more types added, see GENOME_.. above
**********************************************/
NLM_EXTERN Boolean AddGenomeToEntry (
NCBISubPtr submission,
SeqEntryPtr entry ,
Int2 type );
#define SUBSRC_chromosome 1
#define SUBSRC_map 2
#define SUBSRC_clone 3
#define SUBSRC_subclone 4
#define SUBSRC_haplotype 5
#define SUBSRC_genotype 6
#define SUBSRC_sex 7
#define SUBSRC_cell_line 8
#define SUBSRC_cell_type 9
#define SUBSRC_tissue_type 10
#define SUBSRC_clone_lib 11
#define SUBSRC_dev_stage 12
#define SUBSRC_frequency 13
#define SUBSRC_germline 14
#define SUBSRC_rearranged 15
#define SUBSRC_lab_host 16
#define SUBSRC_pop_variant 17
#define SUBSRC_tissue_lib 18
#define SUBSRC_plasmid_name 19
#define SUBSRC_transposon_name 20
#define SUBSRC_insertion_seq_name 21
#define SUBSRC_plastid_name 22
#define SUBSRC_country 23
#define SUBSRC_segment 24
#define SUBSRC_endogenous_virus_name 25
#define SUBSRC_transgenic 26
#define SUBSRC_environmental_sample 27
#define SUBSRC_isolation_source 28
#define SUBSRC_lat_lon 29
#define SUBSRC_collection_date 30
#define SUBSRC_collected_by 31
#define SUBSRC_identified_by 32
#define SUBSRC_fwd_primer_seq 33
#define SUBSRC_rev_primer_seq 34
#define SUBSRC_fwd_primer_name 35
#define SUBSRC_rev_primer_name 36
#define SUBSRC_metagenomic 37
#define SUBSRC_mating_type 38
#define SUBSRC_linkage_group 39
#define SUBSRC_haplogroup 40
#define SUBSRC_whole_replicon 41
#define SUBSRC_phenotype 42
#define SUBSRC_other 255
/*********************************************
* SubSource defines subclasses of source material
* (also see OrgMod below for subclasses of organism names)
*
* allowed values for type are:
chromosome (1) ,
map (2) ,
clone (3) ,
subclone (4) ,
haplotype (5) ,
genotype (6) ,
sex (7) ,
cell-line (8) ,
cell-type (9) ,
tissue-type (10) ,
clone-lib (11) ,
dev-stage (12) ,
frequency (13) ,
germline (14) ,
rearranged (15) ,
lab-host (16) ,
pop-variant (17) ,
tissue-lib (18) ,
plasmid-name (19) ,
transposon-name (20) ,
insertion-seq-name (21) ,
plastid-name (22) ,
country (23) ,
segment (24) ,
endogenous-virus-name (25) ,
transgenic (26) ,
environmental-sample (27) ,
isolation-source (28) ,
lat-lon (29) , -- +/- decimal degrees
collection-date (30) , -- DD-MMM-YYYY format
collected-by (31) , -- name of person who collected the sample
identified-by (32) , -- name of person who identified the sample
fwd-primer-seq (33) , -- sequence (possibly more than one; semicolon-separated)
rev-primer-seq (34) , -- sequence (possibly more than one; semicolon-separated)
fwd-primer-name (35) ,
rev-primer-name (36) ,
metagenomic (37) ,
mating-type (38) ,
linkage-group (39) ,
haplogroup (40) ,
whole-replicon (41) ,
phenotype (42) ,
other (255) } ,
* value is an optional string to give the name (eg. of the
* clone)
******************************************/
NLM_EXTERN Boolean AddSubSourceToEntry (
NCBISubPtr submission,
SeqEntryPtr entry ,
Int2 type ,
CharPtr value);
#define ORGMOD_strain 2
#define ORGMOD_substrain 3
#define ORGMOD_type 4
#define ORGMOD_subtype 5
#define ORGMOD_variety 6
#define ORGMOD_serotype 7
#define ORGMOD_serogroup 8
#define ORGMOD_serovar 9
#define ORGMOD_cultivar 10
#define ORGMOD_pathovar 11
#define ORGMOD_chemovar 12
#define ORGMOD_biovar 13
#define ORGMOD_biotype 14
#define ORGMOD_group 15
#define ORGMOD_subgroup 16
#define ORGMOD_isolate 17
#define ORGMOD_common 18
#define ORGMOD_acronym 19
#define ORGMOD_dosage 20
#define ORGMOD_nat_host 21
#define ORGMOD_sub_species 22
#define ORGMOD_specimen_voucher 23
#define ORGMOD_authority 24
#define ORGMOD_forma 25
#define ORGMOD_forma_specialis 26
#define ORGMOD_ecotype 27
#define ORGMOD_synonym 28
#define ORGMOD_anamorph 29
#define ORGMOD_teleomorph 30
#define ORGMOD_breed 31
#define ORGMOD_gb_acronym 32
#define ORGMOD_gb_anamorph 33
#define ORGMOD_gb_synonym 34
#define ORGMOD_culture_collection 35
#define ORGMOD_bio_material 36
#define ORGMOD_metagenome_source 37
#define ORGMOD_old_lineage 253
#define ORGMOD_old_name 254
#define ORGMOD_other 255
/* Defines for BioSrc.origin
*/
#define ORG_UNKNOWN 0
#define ORG_NATURAL 1
#define ORG_NATMUT 2
#define ORG_MUT 3
#define ORG_ARTIFICIAL 4
#define ORG_SYNTHETIC 5
#define ORG_OTHER 255
#define ORG_DEFAULT ORG_UNKNOWN
#define IS_ORG_UNKNOWN(S) ((S).origin == ORG_UNKNOWN)
#define IS_ORG_NATURAL(S) ((S).origin == ORG_NATURAL)
#define IS_ORG_NATMUT(S) ((S).origin == ORG_NATMUT)
#define IS_ORG_MUT(S) ((S).origin == ORG_MUT)
#define IS_ORG_ARTIFICIAL(S) ((S).origin == ORG_ARTIFICIAL)
#define IS_ORG_SYNTHETIC(S) ((S).origin == ORG_SYNTHETIC)
#define IS_ORG_OTHER(S) ((S).origin == ORG_OTHER)
/*********************************************
* OrgMod defines subclasses of organism names
* (also see SubSource above for subclasses of source material)
*
* allowed values for type are:
strain (2) ,
substrain (3) ,
type (4) ,
subtype (5) ,
variety (6) ,
serotype (7) ,
serogroup (8) ,
serovar (9) ,
cultivar (10) ,
pathovar (11) ,
chemovar (12) ,
biovar (13) ,
biotype (14) ,
group (15) ,
subgroup (16) ,
isolate (17) ,
common (18) ,
acronym (19) ,
dosage (20) , -- chromosome dosage of hybrid
nat-host (21) , -- natural host of this specimen
sub-species (22) ,
specimen-voucher (23) ,
authority (24) ,
forma (25) ,
forma-specialis (26) ,
ecotype (27) ,
synonym (28) ,
anamorph (29) ,
teleomorph (30) ,
breed (31) ,
gb-acronym (32) , -- used by taxonomy database
gb-anamorph (33) , -- used by taxonomy database
gb-synonym (34) , -- used by taxonomy database
culture-collection (35) ,
bio-material (36) ,
metagenome-source (37) ,
old-lineage (253) ,
old-name (254) ,
other (255) } , -- ASN5: old-name (254) will be added to next spec
* value is an optional string to give the name (eg. of the
* varient)
******************************************/
NLM_EXTERN Boolean AddOrgModToEntry (
NCBISubPtr submission,
SeqEntryPtr entry ,
Int2 type ,
CharPtr value);
/********************************************
* Biomol describes the biological type of the molecule
* current values are:
biomol INTEGER {
unknown (0) ,
genomic (1) ,
pre-RNA (2) , -- precursor RNA of any sort really
mRNA (3) ,
rRNA (4) ,
tRNA (5) ,
snRNA (6) ,
scRNA (7) ,
peptide (8) ,
other-genetic (9) , -- other genetic material
genomic-mRNA (10) , -- reported a mix of genomic and cdna sequence
other (255) } DEFAULT unknown ,
********************************************/
NLM_EXTERN Boolean AddBiomolToEntry (
NCBISubPtr submission,
SeqEntryPtr entry ,
Int2 type );
/********************************************
*
* What technique was used to get this sequence ?
* There are a set of defines in objpubd.h for this:
* Current list is:
#define MI_TECH_unknown 0
#define MI_TECH_standard 1
#define MI_TECH_est 2 EST division
#define MI_TECH_sts 3 STS division
#define MI_TECH_survey 4 GSS division
#define MI_TECH_genemap 5 Bioseq is a genetic map
#define MI_TECH_physmap 6 Bioseq is physical map
#define MI_TECH_derived 7 Bioseq is a computed inference
#define MI_TECH_concept_trans 8 conceptual translation
#define MI_TECH_seq_pept 9 peptide sequencing used
#define MI_TECH_both 10 combination of 8 and 9 used
#define MI_TECH_seq_pept_overlap 11 peptides ordered by overlap
#define MI_TECH_seq_pept_homol 12 peptides ordered by homology
#define MI_TECH_concept_trans_a 13 concept trans supplied by author
#define MI_TECH_other 255 doesnt' fit anything
***************************************
* The following are not explicitly in the ASN.1 spec yet
* but can still be legally used as numbers.
* These are for High Throughput Genome Sequences
* htgs_1 - preliminary data. sequence is made of multiple
* contigs with gaps between them. The order of
* the contigs is not known, although for
* convenience they are in an arbitrary order
* htgs_2 - preliminary data. like htgs_1 except the
* order of the contigs is known and the sequence
* reflects the correct order
* htgs_3 - finished data. All annotations are machine
* generated in bulk. Usually this has been placed
* on a map
*
******************************************
#define MI_TECH_htgs_1 14
#define MI_TECH_htgs_2 15
#define MI_TECH_htgs_3 16
**********************************************************/
NLM_EXTERN Boolean AddTechToEntry (
NCBISubPtr submission,
SeqEntryPtr entry ,
Int2 tech );
/********************************************
* How complete is the molecule?
* here are the allowed values:
*
completeness INTEGER {
unknown (0) ,
complete (1) , -- complete biological entity
partial (2) , -- partial but no details given
no-left (3), -- KNOWN missing 5' or NH3 end
no-right (4) , -- KNOWN missing 3' or COOH end
no-ends (5) , -- KNOWN missing both ends
has-left (6) , -- KNOWN has complete 5' or NH3 end
has-right (7) , -- KNOWN has complete 3' or COOH end
other (255) } DEFAULT unknown }
*******************************************/
NLM_EXTERN Boolean AddCompleteToEntry (
NCBISubPtr submission,
SeqEntryPtr entry ,
Int2 complete );
NLM_EXTERN void AddCompleteness(NCBISubPtr submission, SeqEntryPtr sep, SeqFeatPtr sfp);
/**** OBSOLETE!!!! ***********************************************
* DO NOT USE GIBBmethod
* this is subsumed into AddTechToEntry, above
*
****************************************************************/
NLM_EXTERN Boolean AddGIBBmethodToEntry (
NCBISubPtr submission,
SeqEntryPtr entry ,
Int2 method );
#define METHOD_concept_transl 1
#define METHOD_seq_pept 2
#define METHOD_both 3
#define METHOD_seq_pept_overlap 4
#define METHOD_seq_pept_homol 5
#define METHOD_concept_transl_a 6
#define METHOD_other 255
NLM_EXTERN Boolean AddCreateDateToEntry (
NCBISubPtr submission,
SeqEntryPtr entry ,
Int2 month ,
Int2 day ,
Int2 year );
/*************************************************************************
*
* Modifiers modify the meaning of all entries in the set or sequence
* to which they are applied. This is particularly important for
* indicating organelle sequences, RNA genomes, or mutants.
*
* Less obvious is indicating completness.
*
* A genomic sequence is assumed to be partial unless the "complete"
* modifier is used.
* A peptide sequence is assumed to be complete unless the "partial"
* modifier is used.
* A cDNA is assumed to be complete (as well as one can tell) unless
* "partial" is used.
*
* A genomic sequence is assumed to be nuclear unless the "mitochondrial"
* (or other organelle) modifier is used.
* All sequences are assumed to be natural unless "synthetic",
* "recombinant", or "mutagen" are used.
*
*************************************************************************/
/***************************************
* Adds a ValNode of the appropriate type
* to the SeqEntry
* Note that caller must still create the
* specific descriptor structure and attach it to
* the returned ValNode
*
****************************************/
NLM_EXTERN ValNodePtr NewDescrOnSeqEntry (SeqEntryPtr entry, Int2 type);
NLM_EXTERN ValNodePtr GetDescrOnSeqEntry (
SeqEntryPtr entry,
Int2 type);
NLM_EXTERN Boolean AddModifierToEntry (
NCBISubPtr submission,
SeqEntryPtr entry ,
Int2 modifier );
#define MODIF_dna 0
#define MODIF_rna 1
#define MODIF_extrachrom 2
#define MODIF_plasmid 3
#define MODIF_mitochondrial 4
#define MODIF_chloroplast 5
#define MODIF_kinetoplast 6
#define MODIF_cyanelle 7
#define MODIF_synthetic 8 /* synthetic sequence */
#define MODIF_recombinant 9 /* recombinant construct */
#define MODIF_partial 10
#define MODIF_complete 11
#define MODIF_mutagen 12 /* subject of mutagenesis ? */
#define MODIF_natmut 13 /* natural mutant ? */
#define MODIF_transposon 14
#define MODIF_insertion_seq 15
#define MODIF_no_left 16 /* missing left end (5' for na, NH2 for aa) */
#define MODIF_no_right 17 /* missing right end (3' or COOH) */
#define MODIF_macronuclear 18
#define MODIF_proviral 19
#define MODIF_est 20 /* expressed sequence tag */
/*** add/build publications ***/
NLM_EXTERN Boolean AddPubToEntry (
NCBISubPtr submission,
SeqEntryPtr entry ,
PubPtr pub );
NLM_EXTERN PubPtr CitSubBuild ( /* for first data submission **/
NCBISubPtr submission,
Int2 month,
Int2 day,
Int2 year,
Int2 medium );
NLM_EXTERN PubPtr CitSubUpdateBuild ( /* for updates to existing record */
NCBISubPtr submission,
Int2 month,
Int2 day,
Int2 year ,
Int2 medium ,
CharPtr descr ); /* description of update, make it short */
#define MEDIUM_NOT_SET 0
#define MEDIUM_PAPER 1
#define MEDIUM_TAPE 2
#define MEDIUM_FLOPPY 3
#define MEDIUM_EMAIL 4
#define MEDIUM_OTHER 255
NLM_EXTERN PubPtr CitArtBuild (
NCBISubPtr submission,
CharPtr title ,
CharPtr journal ,
CharPtr volume ,
CharPtr issue ,
CharPtr pages ,
Int2 month ,
Int2 day ,
Int2 year ,
Int2 status );
#define PUB_STATUS_PUBLISHED 0
#define PUB_STATUS_SUBMITTED 1
#define PUB_STATUS_IN_PRESS 2
#define PUB_STATUS_UNPUBLISHED 3
/*************************************************************************
*
* Author names can be given in various forms
* You MUST give at least a last name
* You should give at least first name or initials.
* Initials are just for first and middle names, and are
* separated by periods.
*
* example: John Q. Public
* last_name = "Public"
* first_name = "John"
* middle_name = NULL
* initials = "J.Q."
*
*************************************************************************/
NLM_EXTERN Boolean AddAuthorToPub ( /* call once for each author, in order */
NCBISubPtr submission,
PubPtr the_pub,
CharPtr last_name,
CharPtr first_name,
CharPtr middle_name,
CharPtr initials, /* separated by periods, no initial for last name */
CharPtr suffix ); /* Jr. Sr. III */
/*************************************************************************
*
* Author Affiliation
* only one allowed per pub (one per author is also possible, but is
* not supported by this interface )
*
* affil = institutional affiliation
* div = division of institution
* street = street address
* city = city
* sub = subdivision of country (e.g. state.. optional)
* country = country
* postal_code = zip code in the USA
*
*************************************************************************/
NLM_EXTERN Boolean AddAffiliationToPub ( /* call once per pub */
NCBISubPtr submission,
PubPtr the_pub,
CharPtr affil, /* e.g. "Xyz University" */
CharPtr div, /* e.g. "Dept of Biology" */
CharPtr street, /* e.g. "123 Academic Road" */
CharPtr city, /* e.g. "Metropolis" */
CharPtr sub, /* e.g. "Massachusetts" */
CharPtr country , /* e.g. "USA" */
CharPtr postal_code ); /* e.g."02133" */
/*****************************************************************************
*
* Add Features to the entry
* Add location to feature
* Add info for specific types to feature
*
*****************************************************************************/
NLM_EXTERN SeqFeatPtr FeatureBuild (
NCBISubPtr submission,
SeqEntryPtr entry_to_put_feature,
Boolean feature_is_partial,
Uint1 evidence_is_experimental,
Boolean biological_exception,
CharPtr comment );
#define EVIDENCE_NOT_SET 0
#define EVIDENCE_EXPERIMENTAL 1
#define EVIDENCE_NOT_EXPERIMENTAL 2
/*************************************************************************
*
* About feature locations:
* Internally the NCBI software represents locations on sequence as
* offsets from the start of the sequence (i.e. from 0 - (length -1)).
* Also, the "from" position is always <= "to", even for locations on
* the minus strand. Finally, no location can cross the origin of a
* circular sequence.. it must be split in two. This makes routines
* that access locations very consistent and easy to write.
*
* However, most biologists number sequences starting with 1, not 0.
* It is natural to think of a coding region on the minus strand going
* from 5243 to 2993. And it is not unusual to think of the origin of
* replication being from 5344 to 10 on the plus strand of a circular
* sequence.
*
* AddIntervalToFeature and AddPointToFeature were written to support
* the biological notion. They convert to the internal format
* automatically. So, for these two functions:
*
* 1) numbers are in the range 1 - length
* 2) from <= to on plus strand
* to <= from on minus strand
* 3) numbers not conforming to (2) are assumed to go around the origin
* of a circular sequence. It is an error on a linear sequence.
* 4) Intervals should be added in biological order (e.g. exon1, exon2,
* exon3...) no matter which strand the feature is on.
* 5) You must always indicate explicitly the Bioseq the interval is
* on. You may either pass in the SeqEntryPtr or the local_name you
* used when you created the sequence. The sequence must have
* been previously created with AddSeqTo... If you give both the
* SeqEntryPtr and the local_name, they must agree.
* 6) -1 (minus one) is a short hand for "end of sequence". To indicate
* the whole sequence you can give from = 1, to = -1
*
*************************************************************************/
NLM_EXTERN Boolean AddIntervalToFeature (
NCBISubPtr submission,
SeqFeatPtr sfp,
SeqEntryPtr the_seq ,
CharPtr local_name ,
Int4 from ,
Int4 to ,
Boolean on_plus_strand ,
Boolean start_before_from ,
Boolean stop_after_to );
NLM_EXTERN Boolean AddIntToSeqLoc (
SeqLocPtr PNTR old_slp,
Int4 from,
Int4 to,
SeqIdPtr sip,
Int2 fuzz_from,
Int2 fuzz_to,
Int2 strand);
NLM_EXTERN Boolean AddIntToSeqFeat (
SeqFeatPtr sfp,
Int4 from,
Int4 to,
BioseqPtr bsp,
Int2 fuzz_from,
Int2 fuzz_to,
Int2 strand);
NLM_EXTERN Boolean AddPointToFeature (
NCBISubPtr submission,
SeqFeatPtr sfp,
SeqEntryPtr the_seq ,
CharPtr local_name ,
Int4 location ,
Boolean on_plus_strand ,
Boolean is_after_location ,
Boolean is_before_location );
NLM_EXTERN Boolean AddPntToSeqLoc (
SeqLocPtr PNTR p_slp,
Int4 point,
BioseqPtr bsp,
Int2 fuzz,
Int2 strand);
NLM_EXTERN Boolean AddPntToSeqFeat (
SeqFeatPtr sfp,
Int4 point,
BioseqPtr bsp,
Int2 fuzz,
Int2 strand);
/*************************************************************************
*
* Having made a generalized feature, now add type specific info to it.
*
*************************************************************************/
/************************************************************
*
* A comment is the simplest feature. It is required that you
* supplied a "comment" argument to FeatureBuild. In GenBank format
* it will appear as misc_feat, with the comment appearing as the
* \note.
***************************************************************/
NLM_EXTERN Boolean MakeCommentFeature (
NCBISubPtr submission,
SeqFeatPtr feature );
/*****************************************************************
*
* This connects a protein sequence with the nucleic acid
* region which codes for it. So the protein is given as an
* argument, as well as adding intervals on the nucleic acid.
* A complete coding region includes the initial Met codon and
* the final termination codon.
*
*****************************************************************/
NLM_EXTERN Boolean MakeCdRegionFeature (
NCBISubPtr submission,
SeqFeatPtr feature,
Int2 frame ,
Int2 genetic_code , /* see end of this file for genetic codes */
SeqEntryPtr protein_product, /* give id of protein. if NULL, call */
CharPtr local_id_for_protein); /* function below to create by transl */
/******************************************************************
*
* A Code-break allows an exception to be made in the translation
* of a particular codon. You must give positions of the first
* and last bases of the codon in the DNA sequence and the amino
* acid to place there, instead of the normal translation. This
* should be used sparingly, and a comment on the feature should
* explain why it was done.
*
* The location is specified the same as in AddIntervalToFeature.
* AA_for_protein points the amino acid to use, in ncbieaa code.
*
******************************************************************/
NLM_EXTERN Boolean AddCodeBreakToCdRegion (
NCBISubPtr submission,
SeqFeatPtr sfp,
SeqEntryPtr the_seq ,
CharPtr local_name ,
Int4 from ,
Int4 to ,
Boolean on_plus_strand ,
CharPtr AA_for_protein );
/******************************************************************
*
* Special function to make protein from CdRegion feature
*
******************************************************************/
NLM_EXTERN SeqEntryPtr TranslateCdRegion (
NCBISubPtr submission ,
SeqFeatPtr cdregion_feature ,
SeqEntryPtr nuc_prot_entry_to_put_sequence ,
CharPtr local_name , /* for protein sequence */
CharPtr genbank_locus ,
CharPtr genbank_accession ,
Int4 gi_number );
NLM_EXTERN Boolean MakeRNAFeature (
NCBISubPtr submission,
SeqFeatPtr feature,
Int2 rna_type ,
Boolean is_pseudo_gene,
CharPtr rna_name ,
CharPtr AA_for_tRNA ,
CharPtr codon_for_tRNA );
#define RNA_TYPE_premsg 1
#define RNA_TYPE_mRNA 2
#define RNA_TYPE_tRNA 3
#define RNA_TYPE_rRNA 4
#define RNA_TYPE_snRNA 5
#define RNA_TYPE_scRNA 6
#define RNA_TYPE_snoRNA 7
#define RNA_TYPE_ncRNA 8
#define RNA_TYPE_tmRNA 9
#define RNA_TYPE_misc_RNA 10
#define RNA_TYPE_other 255
/******************************************************************
*
* Once you have made a tRNA feature, you may optionally add the
* the location of the anticodon if you know it. This should be
* within the range of the tRNA feature already created, obviously.
*
* the location is specified on the DNA the same as for
* AddIntervalToFeature
*
******************************************************************/
NLM_EXTERN Boolean AddAntiCodonTotRNA (
NCBISubPtr submission,
SeqFeatPtr sfp,
SeqEntryPtr the_seq ,
CharPtr local_name ,
Int4 from ,
Int4 to ,
Boolean on_plus_strand );
NLM_EXTERN Boolean MakeGeneFeature (
NCBISubPtr submission,
SeqFeatPtr feature,
CharPtr gene_symbol_for_locus ,
CharPtr allele ,
CharPtr descriptive_name ,
CharPtr map_location ,
Boolean is_pseudo_gene ,
CharPtr genetic_database ,
CharPtr gene_id_in_genetic_database ,
CharPtr synonym1 ,
CharPtr synonym2 ,
CharPtr synonym3 );
NLM_EXTERN Boolean MakeProteinFeature (
NCBISubPtr submission,
SeqFeatPtr feature ,
CharPtr protein_name1,
CharPtr protein_name2,
CharPtr protein_name3,
CharPtr descriptive_name,
CharPtr ECnum1,
CharPtr ECnum2,
CharPtr activity1,
CharPtr activity2,
CharPtr protein_database,
CharPtr id_in_protein_database);
NLM_EXTERN Boolean MakeRegionFeature (
NCBISubPtr submission,
SeqFeatPtr feature ,
CharPtr region_name );
NLM_EXTERN Boolean MakeSiteFeature (
NCBISubPtr submission,
SeqFeatPtr feature ,
Int2 site_type );
NLM_EXTERN Boolean MakeImpFeature (
NCBISubPtr submission,
SeqFeatPtr feature ,
CharPtr key );
NLM_EXTERN Boolean AddQualToImpFeature (
NCBISubPtr submission,
SeqFeatPtr imp_feature ,
CharPtr qualifier ,
CharPtr value );
NLM_EXTERN Boolean MakePubFeature (
NCBISubPtr submission,
SeqFeatPtr feature,
PubPtr pub );
NLM_EXTERN Boolean AddBasesToByteStore (ByteStorePtr bsp, CharPtr the_bases);
NLM_EXTERN Boolean AddAAsToByteStore (ByteStorePtr bsp, CharPtr the_aas);
/*****************************************************************************
*
* AddPhrapGraph (submission, the_seq, local_name, phrap_values)
* Converts phrap byte array to SeqGraph, wraps in SeqAnnot, adds to Bioseq.
* The length of data in the array must be equal to the length of the Bioseq.
*
*****************************************************************************/
NLM_EXTERN Boolean AddPhrapGraph (
NCBISubPtr submission,
SeqEntryPtr the_seq ,
CharPtr local_name ,
BytePtr phrap_values );
NLM_EXTERN Boolean AddPhrapGraphToSeqLit (
NCBISubPtr submission,
SeqLitPtr slp ,
BytePtr phrap_values );
/* internal functions for reference gene project */
NLM_EXTERN UserObjectPtr CreateRefGeneTrackUserObject (void);
NLM_EXTERN void AddStatusToRefGeneTrackUserObject (UserObjectPtr uop, CharPtr status);
NLM_EXTERN void AddGeneratedToRefGeneTrackUserObject (UserObjectPtr uop, Boolean generated);
NLM_EXTERN void AddCuratorToRefGeneTrackUserObject (UserObjectPtr uop, CharPtr collaborator);
NLM_EXTERN void AddCuratorURLToRefGeneTrackUserObject (UserObjectPtr uop, CharPtr url);
NLM_EXTERN void AddSourceToRefGeneTrackUserObject (UserObjectPtr uop, CharPtr genomicSource);
NLM_EXTERN void AddAccessionToRefGeneTrackUserObject (UserObjectPtr uop, CharPtr field,
CharPtr accn, Int4 gi, Int4 from,
Int4 to, CharPtr comment);
/* experimental function to associate mRNA with protein product in cases of alt splicing */
NLM_EXTERN UserObjectPtr CreateMrnaProteinLinkUserObject (BioseqPtr protbsp);
/* vector screen, validator count, general submission comment user object (JP) */
NLM_EXTERN UserObjectPtr CreateSubmissionUserObject (CharPtr univecComment,
CharPtr additionalComment,
Int4 validatorErrorCount,
Int4 validatorHashCode,
Boolean isCloningVector);
/* clone name and ID for genomic contig RefSeq records */
NLM_EXTERN UserObjectPtr CreateContigCloneUserObject (CharPtr name, Int4 ID);
/* gene ontology process, component, and function user object */
NLM_EXTERN UserObjectPtr CreateGeneOntologyUserObject (
void
);
NLM_EXTERN void AddToGeneOntologyUserObject (
UserObjectPtr uop,
CharPtr type,
CharPtr text,
CharPtr goid,
Int4 pmid,
CharPtr goref,
CharPtr evidence
);
/* model evidence user object */
NLM_EXTERN UserObjectPtr CreateModelEvidenceUserObject (
CharPtr method,
CharPtr contigParent
);
NLM_EXTERN void AddMrnaOrESTtoModelEvidence (
UserObjectPtr uop,
CharPtr type,
CharPtr accn,
Int4 length,
Int4 gaplen
);
NLM_EXTERN UserFieldPtr FindModelEvidenceField (
UserObjectPtr uop,
CharPtr type
);
/* third party accession list user object manipulation */
NLM_EXTERN UserObjectPtr CreateTpaAssemblyUserObject (
void
);
NLM_EXTERN UserFieldPtr CreateTPAAssemblyAccessionField (CharPtr accn);
NLM_EXTERN UserFieldPtr CreateTPAAssemblyFromField (Int4 from);
NLM_EXTERN UserFieldPtr CreateTPAAssemblyToField (Int4 to);
NLM_EXTERN void AddAccessionToTpaAssemblyUserObject (
UserObjectPtr uop,
CharPtr accn,
Int4 from,
Int4 to
);
NLM_EXTERN UserObjectPtr CreateGenomeProjectsDBUserObject (
void
);
NLM_EXTERN UserObjectPtr AddIDsToGenomeProjectsDBUserObject (
UserObjectPtr uop,
Int4 projectID,
Int4 parentID
);
/* annot desc comment policy user object */
NLM_EXTERN UserObjectPtr CreateAnnotDescCommentPolicyUserObject (
Boolean showInCommentBlock
);
/* feature fetch policy user object */
NLM_EXTERN UserObjectPtr CreateFeatureFetchPolicyUserObject (
CharPtr policy
);
/* structured comment user object for flatfile presentation */
NLM_EXTERN UserObjectPtr CreateStructuredCommentUserObject (
CharPtr prefix,
CharPtr suffix
);
NLM_EXTERN void AddItemStructuredCommentUserObject (
UserObjectPtr uop,
CharPtr field,
CharPtr str
);
/* DBLink user object for flatfile presentation */
NLM_EXTERN UserObjectPtr CreateDBLinkUserObject (
void
);
NLM_EXTERN void AddTraceAssemblyIDsToDBLinkUserObject (
UserObjectPtr uop,
Int4 num,
Int4Ptr values
);
NLM_EXTERN void AddBioSampleIDsToDBLinkUserObject (
UserObjectPtr uop,
Int4 num,
CharPtr PNTR values
);
NLM_EXTERN void AddSeqReadArchIDsToDBLinkUserObject (
UserObjectPtr uop,
Int4 num,
CharPtr PNTR values
);
NLM_EXTERN void AddFieldsToDBLinkUserObject (
UserObjectPtr uop,
CharPtr field_name,
Int4 num,
CharPtr PNTR values
);
NLM_EXTERN void AddProbeDBIDsToDBLinkUserObject (
UserObjectPtr uop,
Int4 num,
CharPtr PNTR values
);
NLM_EXTERN void AddSeqReadArchiveIDsToDBLinkUserObject (
UserObjectPtr uop,
Int4 num,
CharPtr PNTR values
);
NLM_EXTERN void AddBioProjectIDsToDBLinkUserObject (
UserObjectPtr uop,
Int4 num,
CharPtr PNTR values
);
/* NcbiCleanup user object for SeriousSeqEntryCleanup time/version stamp */
NLM_EXTERN UserObjectPtr CreateNcbiCleanupUserObject (
void
);
NLM_EXTERN void AddStringToNcbiCleanupUserObject (
UserObjectPtr uop,
CharPtr field,
CharPtr str
);
NLM_EXTERN void AddIntegerToNcbiCleanupUserObject (
UserObjectPtr uop,
CharPtr field,
Int4 num
);
/* FindNcbiCleanupUserObject returns user object on top Seq-entry */
NLM_EXTERN UserObjectPtr FindNcbiCleanupUserObject (
SeqEntryPtr sep
);
NLM_EXTERN void RemoveAllNcbiCleanupUserObjects (
SeqEntryPtr sep
);
/* Also can put NcbiCleanupUserObject on Seq-annot Annot-desc */
NLM_EXTERN UserObjectPtr FindSeqAnnotCleanupUserObj (
SeqAnnotPtr sap
);
NLM_EXTERN void RemoveAllSeqAnnotCleanupUserObjs (
SeqAnnotPtr sap
);
NLM_EXTERN UserObjectPtr FindNcbiAutofixUserObject (
SeqEntryPtr sep
);
NLM_EXTERN void AddNcbiAutofixUserObject (
SeqEntryPtr sep
);
NLM_EXTERN void RemoveNcbiAutofixUserObjects (
SeqEntryPtr sep
);
/* Mark unverified sequences */
NLM_EXTERN UserObjectPtr CreateUnverifiedUserObject (
void
);
NLM_EXTERN UserObjectPtr FindUnverifiedUserObject (
SeqEntryPtr sep
);
NLM_EXTERN UserObjectPtr AddUnverifiedUserObject (
SeqEntryPtr sep
);
NLM_EXTERN UserObjectPtr AddUnverifiedUserObjectToBioseq (
BioseqPtr bsp
);
NLM_EXTERN UserObjectPtr AddUnverifiedUserObjectToBioseqParent (
BioseqPtr bsp
);
NLM_EXTERN void AddStringToUnverifiedUserObject (
UserObjectPtr uop,
CharPtr field,
CharPtr str
);
NLM_EXTERN void RemoveUnverifiedUserObjects (
SeqEntryPtr sep
);
NLM_EXTERN Boolean IsUnverifiedUserObject (
UserObjectPtr uop
);
#ifdef __cplusplus
}
#endif
#undef NLM_EXTERN
#ifdef NLM_EXPORT
#define NLM_EXTERN NLM_EXPORT
#else
#define NLM_EXTERN
#endif
#endif
/*****************************************************************************
*
* Allowed IUPAC nucleic acid codes from /ncbi/data/seqcode.prt
*
( symbol "A", name "Adenine" ),
( symbol "B" , name "G or T or C" ),
( symbol "C", name "Cytosine" ),
( symbol "D", name "G or A or T" ),
( symbol "G", name "Guanine" ),
( symbol "H", name "A or C or T" ) ,
( symbol "K", name "G or T" ),
( symbol "M", name "A or C" ),
( symbol "N", name "A or G or C or T" ) ,
( symbol "R", name "G or A"),
( symbol "S", name "G or C"),
( symbol "T", name "Thymine"),
( symbol "V", name "G or C or A"),
( symbol "W", name "A or T" ),
( symbol "Y", name "T or C")
*
*
*****************************************************************************/
/*****************************************************************************
*
* Allowed IUPAC amino acid codes from /ncbi/data/seqcode.prt
( symbol "A", name "Alanine" ),
( symbol "B" , name "Asp or Asn" ),
( symbol "C", name "Cysteine" ),
( symbol "D", name "Aspartic Acid" ),
( symbol "E", name "Glutamic Acid" ),
( symbol "F", name "Phenylalanine" ),
( symbol "G", name "Glycine" ),
( symbol "H", name "Histidine" ) ,
( symbol "I", name "Isoleucine" ),
( symbol "J", name "Leu or Ile" ),
( symbol "K", name "Lysine" ),
( symbol "L", name "Leucine" ),
( symbol "M", name "Methionine" ),
( symbol "N", name "Asparagine" ) ,
( symbol "O", name "Pyrrolysine" ),
( symbol "P", name "Proline" ),
( symbol "Q", name "Glutamine"),
( symbol "R", name "Arginine"),
( symbol "S", name "Serine"),
( symbol "T", name "Threoine"),
{ symbol "U", name "Selenocysteine"},
( symbol "V", name "Valine"),
( symbol "W", name "Tryptophan" ),
( symbol "X", name "Undetermined or atypical"),
( symbol "Y", name "Tyrosine"),
( symbol "Z", name "Glu or Gln" )
*
*
*****************************************************************************/
/*****************************************************************************
*
* Genetic Code id's and names from /ncbi/data/gc.prt
* gc.prt lists the legal start codons and genetic codes fully
*
name "Standard" ,
id 1 ,
name "Vertebrate Mitochondrial" ,
id 2 ,
name "Yeast Mitochondrial" ,
id 3 ,
name "Mold Mitochondrial and Mycoplasma" ,
id 4 ,
name "Invertebrate Mitochondrial" ,
id 5 ,
name "Ciliate Macronuclear and Daycladacean" ,
id 6 ,
name "Echinoderm Mitochondrial" ,
id 9 ,
name "Euplotid Macronuclear" ,
id 10 ,
name "Bacterial and Plant Plastid" ,
id 11 ,
name "Alternative Yeast Nuclear" ,
id 12 ,
name "Ascidian Mitochondrial" ,
id 13 ,
name "Alternative Flatworm Mitochondrial" ,
id 14 ,
name "Blepharisma Macronuclear" ,
id 15 ,
name "Chlorophycean Mitochondrial" ,
id 16 ,
name "Trematode Mitochondrial" ,
id 21 ,
name "Scenedesmus obliquus Mitochondrial" ,
id 22 ,
name "Thraustochytrium Mitochondrial" ,
id 23 ,
*
*
*****************************************************************************/
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