/usr/bin/fasta2frag is in mira-assembler 4.0-1.
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# \
exec tclsh "$0" ${1+"$@"}
#
# Written by Bastien Chevreux (BaCh)
#
# Copyright (C) 2004 and later by Bastien Chevreux
#
# All rights reserved.
#
# This program is free software; you can redistribute it and/or
# modify it under the terms of the GNU General Public License
# as published by the Free Software Foundation; either version 2
# of the License, or (at your option) any later version.
#
# This program is distributed in the hope that it will be useful,
# but WITHOUT ANY WARRANTY; without even the implied warranty of
# MERCHANTABILITY or FITNESS FOR A PARTICULAR PURPOSE. See the
# GNU General Public License for more details.
#
# You should have received a copy of the GNU General Public License
# along with this program; if not, write to the
# Free Software Foundation, Inc.,
# 51 Franklin Street, Fifth Floor, Boston, MA 02110-1301, USA
#
#
#set min 3
#set max 7
#for {set i 0} {$i< 100} {incr i} {
# set nummut [expr {$min+int(rand()*($max-$min+1))}]
# puts $nummut
#}
#exit
namespace eval fasta2frag {
variable opts
}
proc string_reverse str {
set res {}
set i [string length $str]
while {$i > 0} {append res [string index $str [incr i -1]]}
set res
}
proc list_reverse list {
set _temp {}
for {set i [ expr [ llength $list ] - 1 ] } {$i >= 0} {incr i -1} {
lappend _temp [ lindex $list $i ]
}
return $_temp
}
proc fasta2frag::dnamut_basechange {dnaseq} {
set lenseq [string length $dnaseq]
set cpos [expr {int(rand()*$lenseq)}]
set actbase [string index $dnaseq $cpos]
set tmp [expr {int(rand()*3)}]
set i 0
foreach base {a c g t} {
if {$base != $actbase} {
if {$i == $tmp} {
set newbase [string toupper $base]
}
incr i
}
}
puts "oldseq: $dnaseq"
set dnaseq [string replace $dnaseq $cpos $cpos $newbase]
puts "newseq: $dnaseq"
return $dnaseq
}
proc fasta2frag::dnamut_insert {dnaseq} {
set lenseq [string length $dnaseq]
set inspos [expr {int(rand()*$lenseq)}]
set tmp [expr {int(rand()*4)}]
set inswhat "[string index $dnaseq $inspos][lindex {a c g t} $tmp]"
puts "insert: $insbase"
set dnaseq [string replace $dnaseq $inspos $inspos $inswhat]
return $dnaseq
}
proc fasta2frag::dnamut_delete {dnaseq} {
set lenseq [string length $dnaseq]
set delpos [expr {int(rand()*$lenseq)}]
set dnaseq [string replace $dnaseq $delpos $delpos]
return $dnaseq
}
proc fasta2frag::dnamut {dnaseq min max} {
set nummut [expr {$min+int(rand()*($max-$min+1))}]
for {set i 1} {$i <= $nummut} {incr i} {
puts "mut $i"
#set dnaseq [dnamut_basechange $dnaseq]
#set muttype [expr {int(rand()*3)}]
#switch -exact -- $muttype {
# 0 { set $dnaseq [dnamut_basechange $dnaseq] }
# 1 { set $dnaseq [dnamut_insert $dnaseq] }
# 2 { set $dnaseq [dnamut_delete $dnaseq] }
#}
}
return $dnaseq
}
proc fasta2frag::dumpfasta {name descline dnaseq fout qualseq qout} {
variable opts
if {$opts(-minmut) || $opts(-maxmut)} {
set dnaseq [dnamut $dnaseq $opts(-minmut) $opts(-maxmut)]
}
puts $fout ">$name $descline\n$dnaseq"
if {[llength $qualseq]} {
puts $qout ">$name\n$qualseq"
}
}
#proc fasta2frag::getdnafromto {dnaseq from to} {
# variable opts
#
# set retseq ""
#
# set dnalen [string length $dnaseq]
#
# set totalbases 0
# set len [expr {$from - $to}]
# set ii 0
#
# for {} {$totalbases < $len} {incr ii} {
# set realindex [expr {($from+$ii)%$dnalen}]
#
# append retseq [string index $dnaseq $realindex ]
# if {[llength $quals]>0} {
# lappend retquals [lindex $quals $realindex]
# } else {
# lappend retquals $opts(-q)
# }
# }
#}
proc fasta2frag::getqualfromto {dnaseq quals from to} {
variable opts
set qualslen [llength $quals]
set qualseq {}
if {$qualslen > 0} {
for {set i $from} {$i < $to} {incr i} {
set thisqual -1
catch {
set thisqual [expr {int([lindex $quals [expr {$i%$qualslen}] ] / $opts(-qualdivisor))}]
}
# noqual?
if {$thisqual < 0} {
set thisqual $opts(-minqual)
}
if {$thisqual < $opts(-minqual)} {
set thisqual $opts(-minqual)
}
lappend qualseq $thisqual
}
} else {
for {set i $from} {$i < $to} {incr i} {
lappend qualseq $opts(-q)
}
}
if {[llength $qualseq] > [string length $dnaseq]} {
set qualseq [lrange $qualseq 1 [string length $dnaseq]]
}
return $qualseq
}
proc fasta2frag::reverse_seq_qual {s q} {
upvar $s dnaseq
upvar $q qualseq
set dnaseq [string map {a t A T c g C G g c G C t a T A } [string_reverse $dnaseq]]
set qualseq [list_reverse $qualseq]
}
proc fasta2frag::fragASeq {nonamedata name fout quals qout mpout mbout} {
variable opts
#set fid [open $opts(-infile) r]
#set data [read $fid]
#close $fid
puts "fragging $name"
#if {[regsub -all -line {^>(.*?)$} $data "" nonamedata] >1} {
# puts stderr "More than one sequence in fasta file, aborting."
# exit 500
#}
regsub -all {\n} $nonamedata "" data
unset nonamedata
# when circularising is on, append first $opts(-l)-1 bases
# of sequence to end of sequence (and also quals if present)
# if strobing, also add $opts(-l)-$opts(-strobeoff) bases
if {$opts(-c) > 0} {
puts -nonewline "Circularising ..."
set endpos [expr {$opts(-l)-2}]
if {$opts(-s) > 0} {
puts -nonewline " with strobe settings ..."
set endpos [expr {$endpos + ($opts(-l)-2 - $opts(-strobeoff))}]
}
#puts [string range $data 0 $endpos]
append data [string range $data 0 $endpos]
if {[llength $quals] > 0} {
set quals [concat $quals [lrange $quals 0 $endpos]]
}
puts " done."
}
set datalen [string length $data]
set from $opts(-startoffset)
set to $opts(-l)
if {$to > $datalen} {
set to $datalen
}
switch -exact -- $opts(-pairednaming) {
454 {
set fwdname "_pe.f"
set revname "_pe.r"
}
solexa {
set fwdname "_pe/1"
set revname "_pe/2"
}
tigr {
set fwdname "TF"
set revname "TR"
}
sanger {
set fwdname "_pe.p1"
set revname "_pe.q1"
}
default {
error "Unrecognised -pairednaming $opt(-pairednaming)"
}
}
set seqid 1
# of we reach the end of the sequence, this will be set to 1
set lastflag 0
proc putz {bla} {
puts $bla
}
proc random {{range 100}} {
return [expr {25+int(rand()*$range)}]
}
proc getFragLen {from } {
variable opts
#return [expr {$from+[random $opts(-l)]*2}]
return [expr {$from+$opts(-l)}]
}
#for { } {$from < $datalen} { incr from $opts(-i); incr to $opts(-i); incr seqid}
for { } {$from < $datalen} { incr from $opts(-i); incr seqid} {
#set to [expr {$from+$opts(-l)}]
set to [getFragLen $from]
if {$lastflag == 0} {
#puts "$from $to"
if {$to >= $datalen} {
set lastflag 1
}
if {$opts(-p) > 0 } {
set pairnamef ${name}_${seqid}${fwdname}
set pairnamer ${name}_${seqid}${revname}
if { $opts(-s) > 0 } {
error "forget about that strobe thingy"
} else {
set to2 [expr {$from + $opts(-insert_size)}]
set from2 [expr {$to2 - $opts(-l)}]
if {$from2 <= $datalen} {
if {$to > $datalen} {
set to $datalen
}
if {$to2 > $datalen} {
set to2 $datalen
}
set rev1 0
set rev2 0
if { [expr {$seqid % 2}] == 0 } {
switch -exact -- $opts(-r) {
FF { }
RF { set rev1 1}
FR { set rev2 1}
RR { set rev1 1; set rev2 1 }
default { error "-r $opts(-r) is not known, please use FF, RR, FR, RF."}
}
} else {
set tmp $pairnamef
set pairnamef $pairnamer
set pairnamer $tmp
switch -exact -- $opts(-r) {
FF { set rev1 1; set rev2 1 }
RF { set rev1 1}
FR { set rev2 1}
RR { }
default { error "-r $opts(-r) is not known, please use FF, RR, FR, RF."}
}
}
#putz "$pairnamef $rev1\t$pairnamer $rev2"
set dnaseq [string range $data $from [expr {$to-1}]]
set qualseq [getqualfromto $dnaseq $quals $from $to]
#puts "quals: $quals"
#puts "dnaqualseq: $qualseq"
set descline "[expr {$opts(-insert_size)-$opts(-insert_stdev)}] $opts(-insert_size) [expr {$opts(-insert_size)+$opts(-insert_stdev)}] 1 [string length $dnaseq]"
if {$rev1} {
reverse_seq_qual dnaseq qualseq
}
#putz "$pairnamef $rev1 $dnaseq"
dumpfasta $pairnamef$opts(-namesuffix) $descline $dnaseq $fout $qualseq $qout
if {$seqid == 1} {
# if we are working with reversing sequences,
# force a reverse of the sequence
if { $opts(-r) != "FF" } {
reverse_seq_qual dnaseq qualseq
}
dumpfasta ${name}$opts(-namesuffix)_${seqid}_a $descline $dnaseq $fout $qualseq $qout
}
set dnaseq [string range $data $from2 [expr {$to2-1}]]
set qualseq [getqualfromto $dnaseq $quals $from2 $to2]
if {$rev2} {
reverse_seq_qual dnaseq qualseq
}
#putz "$pairnamer $rev2 $dnaseq"
dumpfasta $pairnamer$opts(-namesuffix) $descline $dnaseq $fout $qualseq $qout
puts $mpout "$pairnamef\t$pairnamer"
puts $mbout "$pairnamef\t$pairnamer\tsimplepair"
}
}
} else {
set dnaseq [string range $data $from [expr {$to-1}]]
set qualseq [getqualfromto $dnaseq $quals $from $to]
if { $opts(-r) != "FF" } {
if { [expr {$seqid % 2}] == 0} {
reverse_seq_qual dnaseq qualseq
}
}
set descline "1 [string length $dnaseq]"
dumpfasta ${name}$opts(-namesuffix)_$seqid $descline $dnaseq $fout $qualseq $qout
# the very first and very last fragment will be put twice
# into the data set so that every part of the contig
# is covered at least twice
if {$seqid == 1 || $lastflag >0 } {
# if we a re working with reversing sequences,
# force a reverse of the sequence
if { $opts(-r) != "FF" } {
reverse_seq_qual dnaseq qualseq
}
dumpfasta ${name}$opts(-namesuffix)_${seqid}_a $descline $dnaseq $fout $qualseq $qout
}
}
}
}
}
proc fasta2frag::loadNextQuals {qin} {
variable tempqualname
set quals {}
while {[gets $qin line] != -1} {
if {[string compare [string index $line 0] ">"] == 0} {
set tempqualname "[string map {> ""} [lindex $line 0]]"
return $quals
} else {
set quals [concat $quals $line]
}
}
append quals $line
return $quals
}
proc fasta2frag::processit {} {
variable opts
variable tempqualname
set fin [open $opts(-infile) r]
set fout [open $opts(-outfile) w]
set havequal 0
if {[file exist ${opts(-infile)}.qual]} {
puts "have qual"
set havequal 1
set qin [open ${opts(-infile)}.qual r]
} else {
puts "no ${opts(-infile)}.qual"
#set qout [open /dev/null w]
}
set qout [open ${opts(-outfile)}.qual w]
set mpout ""
set mbout ""
if { $opts(-p) > 0 } {
set mpout [open $opts(-outfile).pairs w]
set mbout [open $opts(-outfile).bambus w]
puts $mbout "library\tsimplepair\t[expr {$opts(-insert_size)-3*$opts(-insert_stdev)}]\t[expr {$opts(-insert_size)+3*$opts(-insert_stdev)}]"
}
gets $fin data
set seqname "[string map {> ""} [lindex $data 0]]"
if {$havequal} {
gets $qin data
set tempqualname "[string map {> ""} [lindex $data 0]]"
}
set actseq ""
set cid 1
while {[gets $fin line] != -1} {
if {[string compare [string index $line 0] ">"] == 0} {
set quals {}
if {$havequal} {
if {$tempqualname != $seqname} {
error "$seqname in fasta file is not equal to $tempqualname in quality file."
}
set quals [loadNextQuals $qin]
}
fragASeq $actseq $seqname $fout $quals $qout $mpout $mbout
incr cid
set actseq ""
set seqname "[string map {> ""} [lindex $line 0]]"
} else {
append actseq $line
}
}
if {[string length $actseq] >0} {
set quals {}
if {$havequal} {
if {$tempqualname != $seqname} {
error "$seqname in fasta file is not equal to $tempqualname in quality file."
}
set quals [loadNextQuals $qin]
}
fragASeq $actseq $seqname $fout $quals $qout $mpout $mbout
}
close $fin
if { $opts(-p) > 0 } {
close $mbout
close $mpout
}
}
proc fasta2frag::sanitycheck {} {
variable opts
}
proc fasta2frag::parsequick {qstr} {
variable opts
}
proc usage {prgname} {
puts stderr "$prgname: Splits a single fasta sequence into several
overlapping fragments.\n"
puts stderr "Usage: $prgname ?options? infile outfile
\t-quick string ''
\t-l int Length of fragments (default=3000)
\t-i int Increment of fragment start site (default=2500)
\t-p int Paired reads (default=0 is off, 1 is on)
\t-r string In shotgun: 'FF' to not to reverse every second read
\t In paired reads mode:
FF: forward-forward
RR: reverse-reverse (Ion Torrent, 454)
FR: forward-reverse (Solexa paired-end)
RF: reverse-forward (Solexa mate-pair)
\t-s int Strobe sequencing (default=0 is off, 1 is on)
\t-q int Default quality when no quality data present (default=30)
\t-c int Circularise fragments so that they form a ring
(default=0 is is off, 1 would be on)
\t-qualdivisor int Divide quality values by this (default=1)
\t-minqual int But give it at least this qual (default=0)
\t-insert_size int paired-end: insert size (default=3000)
\t-insert_stdev int paired-end: standard dev (default=900)
\t this is not working at the moment
\t-pairednaming string naming scheme for paired-end:
\t sanger, tigr, 454 or solexa (default)
\t-minmut int min. number of mutations/seq. errors (def=0)
\t-maxmut int max. number of mutations/seq. errors (def=0)
\t-strobeon int number of bases read during strobe on
\t-strobeoff int number of bases during strobe off
\t-startoffset int start at offset position
\t-namesuffix string suffix name with string
"
exit
}
set fasta2frag::opts(-l) 3000
set fasta2frag::opts(-i) 2500
set fasta2frag::opts(-r) FR
set fasta2frag::opts(-p) 0
set fasta2frag::opts(-s) 0
set fasta2frag::opts(-q) 30
set fasta2frag::opts(-c) 0
#set fasta2frag::opts(-minmut) 1
#set fasta2frag::opts(-maxmut) 2
set fasta2frag::opts(-minmut) 0
set fasta2frag::opts(-maxmut) 0
set fasta2frag::opts(-pairednaming) solexa
set fasta2frag::opts(-qualdivisor) 1
set fasta2frag::opts(-minqual) 0
set fasta2frag::opts(-insert_size) 3000
set fasta2frag::opts(-insert_stdev) 900
set fasta2frag::opts(-infile) ""
set fasta2frag::opts(-outfile) ""
set fasta2frag::opts(-strobeon) 100
set fasta2frag::opts(-strobeoff) 100
set fasta2frag::opts(-startoffset) 0
set fasta2frag::opts(-namesuffix) ""
foreach {key val} $argv {
if {![info exists fasta2frag::opts($key)]} {
if {[string compare [string index $key 0] "-"] == 0} {
puts stderr "Bad key $key\n"
usage $argv0
}
set val $key
set key -infile
}
if { $key == "-quick" } {
fasta2frag::parsequick $val
}
set fasta2frag::opts($key) $val
}
if {[string length $fasta2frag::opts(-infile)] ==0} {
puts "Missing '-infile' as keyword"
usage $argv0 ;
}
if {[string length $fasta2frag::opts(-outfile)] ==0} {
puts "Missing '-outfile' as keyword"
usage $argv0 ;
}
fasta2frag::sanitycheck
fasta2frag::processit
|