ANGSD: Analysis of next generation Sequencing Data

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=Wiki doc=
# write how on website
# write how on website


#Thetas,Tajima,Neutrality test needs documentation and examples files
#Thetas,Tajima,Neutrality test needs documentation and examples files


 
=Code fix=
#doMajorMinor 4 fjerner sites som ikke har major/minor som ref. total maerkeligt og fucked up
#doMajorMinor 4 fjerner sites som ikke har major/minor som ref. total maerkeligt og fucked up
#user custom class missing
#user custom class missing

Revision as of 13:18, 5 March 2014

Wiki doc

  1. write how on website
  1. Thetas,Tajima,Neutrality test needs documentation and examples files

Code fix

  1. doMajorMinor 4 fjerner sites som ikke har major/minor som ref. total maerkeligt og fucked up
  2. user custom class missing
  1. -samglfclean not documented
  1. soap usage is not documented


  1. -sites does not work without all chromsomes being in the *sites file
  2. -sites gives wrong chromomosome in error


  1. make haploid 1dsfs
  2. fix wiki doc with -sites should contain -rf with curs from -sites
  3. describe -trim! does trim 3 remove the first and last 3 bases? or just 2?
  4. from morten shitoutput

h1 h2 h3 = 7 10 5 has less than 3 blocks. skipping h1 h2 h3 = 8 10 5 has less than 3 blocks. skipping h1 h2 h3 = 10 11 5 has less than 3 blocks. skipping h1 h2 h3 = 7 12 5 has less than 3 blocks. skipping h1 h2 h3 = 10 12 5 has less than 3 blocks. skipping h1 h2 h3 = 10 13 5 has less than 3 blocks. skipping h1 h2 h3 = 10 15 5 has less than 3 blocks. skipping h1 h2 h3 = 7 10 6 has less than 3 blocks. skipping h1 h2 h3 = 8 10 6 has less than 3 blocks. skipping h1 h2 h3 = 9 10 6 has less than 3 blocks. skipping h1…

  1. fix -doFasta for single chromosomes. put gzwrite && bufstr.l =0 whenever we change cur
  1. -doMaf 4 is not working if post is not external
  1. Regarding an open issue of printing %e instead o numbers, using the bombyx/lyca dataset:
  1. fix }else{
   fprintf(stderr,"./a.out [make_bed|do_stat|validate_bed|print]\n");
 }  in thetaStat
  1. simplefy filereading. from glf files
  1. check 1offseted in -sites file
  2. add more info to -sites file output
  1. better screen output if unsorted filtering


Anders changes to version 583

1) Default minMaf set to -1 (instead of 0)

2) added

 freqs->freq = new double[pars->numSites]; 

to phatLoop

added the if part of if(freq->freq==NULL)

 freq->freq = new double[pars->numSites]; 

to postFreq and likeFreq funcitons to stop leak + be able to run phat without postFreq/likeFreq

3) changed doMajorMinor 2 to choose a minor allele even if no minor allele is observed (if -minMaf is chosen the site will be removed). This avoid removing side through the majorMinorMod function. The change else if (bases[i]>temp){ -> else if (bases[i]>=temp){ in majorMinorCounts

4) Estimate nInd even if -minInd 0. Else the output is wrong when -minInd 0 filter::run changed

e.g.

$ANG -out out -doMajorMinor 2 -doMaf 8 -bam bam.filelist -doCounts 1 -r 1: before gunzip -c out.mafs.gz | headchromo position major minor phat nInd

1 13999919 A T 0.000000 10

1 13999920 G T 0.000000 10

1 13999921 G T 0.000000 10

1 13999922 C T 0.000000 10

after chromo position major minor phat nInd

1 13999919 A T 0.000000 1

1 13999920 G T 0.000000 1

1 13999921 G T 0.000000 1

1 13999922 C T 0.000000 1

1 13999923 A T 0.000000 1

(there is only information for one individual)