Skip to main content
  • Home
  • Development
  • Documentation
  • Donate
  • Operational login
  • Browse the archive

swh logo
SoftwareHeritage
Software
Heritage
Archive
Features
  • Search

  • Downloads

  • Save code now

  • Add forge now

  • Help

Revision 5c340d6fa70c3f1a711daaf5eefd1cd6aacd9497 authored by Amin Haghani on 20 July 2023, 21:45:10 UTC, committed by GitHub on 20 July 2023, 21:45:10 UTC
Add files via upload
1 parent 6f83fb1
  • Files
  • Changes
  • c10648e
  • /
  • CMAPS_source
  • /
  • parseMAF.py
Raw File Download

To reference or cite the objects present in the Software Heritage archive, permalinks based on SoftWare Hash IDentifiers (SWHIDs) must be used.
Select below a type of object currently browsed in order to display its associated SWHID and permalink.

  • revision
  • directory
  • content
revision badge
swh:1:rev:5c340d6fa70c3f1a711daaf5eefd1cd6aacd9497
directory badge
swh:1:dir:db83229f7017e69c20115f1fd07d9a9dfb14603b
content badge
swh:1:cnt:083a0d5df33ff3bdd8260aeccd10e85e6e4e1324

This interface enables to generate software citations, provided that the root directory of browsed objects contains a citation.cff or codemeta.json file.
Select below a type of object currently browsed in order to generate citations for them.

  • revision
  • directory
  • content
Generate software citation in BibTex format (requires biblatex-software package)
Generating citation ...
Generate software citation in BibTex format (requires biblatex-software package)
Generating citation ...
Generate software citation in BibTex format (requires biblatex-software package)
Generating citation ...
parseMAF.py
import gzip
import sys
from collections import defaultdict
from Bio.Seq import Seq

def main():
    if len(sys.argv) < 7:
        print("Usage: python createMAFFeatures.py <alignment file> <species names file> <output file> <chromosome> <reference species> <reference species chromosome length file>")
        exit(1)
    mafFile = sys.argv[1]
    speciesFile = open(sys.argv[2], 'r')
    featFile = sys.argv[3]
    chr = sys.argv[4]
    refSpecies = sys.argv[5] + "." + chr
    chromLengths = sys.argv[6]

    f = gzip.open(mafFile, 'rb')
    o = gzip.open(featFile, 'w')
    chromSizes = open(chromLengths, 'r')

    species = []
    for line in speciesFile:
        species.append(line.strip())
    species = sorted(species)
    print species

    chrLength = {}
    for line in chromSizes:
        splitLine = line.strip().split()
        chrLength[splitLine[0]] = int(splitLine[1])

    idx = 0
    # write header to output file
    o.write("pos")
    for sp in species:
        o.write("," + sp)
    o.write("\n")

    f.readline() # read header line
    scoreLine = f.readline()
    while scoreLine[0] == '#':
        scoreLine = f.readline()

    numBases = 0
    covered = {} # dictionary of bases covered to account for blocks convering duplicate pieces
    while scoreLine != "":
        sequenceLine = f.readline()
        startHuman = -1
        seqHuman = ""
        alignedToHuman = {}

        lastAlignment = []
        reverseComplement = False
        # parse an alignment block
        while sequenceLine != "\n":
            lastAlignment.append(sequenceLine)
            splitSeq = sequenceLine.split()

            type = splitSeq[0]
            if type == 's':
                curSpecies = splitSeq[1]
                
                if curSpecies == refSpecies: # store info for human
                    trueLenHuman = int(splitSeq[3])
                    if splitSeq[4] == '-': # reverse complement
                        startHuman = chrLength[chr] - int(splitSeq[2]) - trueLenHuman
                        seqHuman = Seq(splitSeq[6].upper()).reverse_complement()
                        reverseComplement=True
                    else:
                        startHuman = int(splitSeq[2])
                        seqHuman = splitSeq[6].upper()
                    lenHumanDash = len(seqHuman)
                else:
                    curSeq = ""
                    if reverseComplement:
                        curSeq = Seq(splitSeq[6].upper()).reverse_complement()
                    else:
                        curSeq = splitSeq[6].upper()
                    alignedToHuman[curSpecies[:curSpecies.find(".")]] = curSeq # store the aligned sequence in other species
            sequenceLine = f.readline()

        # when done with an alignment block go through and output whether each species is the same as the reference species
        pos = startHuman
        for i in range(lenHumanDash):
            if seqHuman[i] != '-':
                numBases += 1
                if not (pos in covered):
                    o.write(str(pos) + "," + seqHuman[i])
                    for sp in species:
                        if (sp not in alignedToHuman) or (alignedToHuman[sp][i] == '-'):
                            o.write(",X")
                        else:
                            o.write("," + str(alignedToHuman[sp][i]))
                    o.write("\n")
                    covered[pos] = 1
                pos += 1

        scoreLine = f.readline()
    o.close()
main()


The diff you're trying to view is too large. Only the first 1000 changed files have been loaded.
Showing with 0 additions and 0 deletions (0 / 0 diffs computed)
swh spinner

Computing file changes ...

back to top

Software Heritage — Copyright (C) 2015–2026, The Software Heritage developers. License: GNU AGPLv3+.
The source code of Software Heritage itself is available on our development forge.
The source code files archived by Software Heritage are available under their own copyright and licenses.
Terms of use: Archive access, API— Content policy— Contact— JavaScript license information— Web API