lh3/bgt

Issues

• Compatibility with GLNexus joint called VCFs

  #17 opened 10 months ago by biojiangke
  0

• BGT issue with Multi Allelic Variant Sites

  #16 opened 3 years ago by rick-heig
  0

• FMF query

  #15 opened 3 years ago by zmaroti
  0

• BGT missing SNPs

  #12 opened 7 years ago by biojiangke
  1

• annotation of output

  #14 opened 3 years ago by zmaroti
  0

• [W::vcf_parse1] can't find '10' in the sequence dictionary

  #13 opened 4 years ago by SmDonkey
  3

• query based on file contents

  #8 opened 6 years ago by mcshane
  0

• Import VCF into existing bgt file

  #11 opened 8 years ago by sndrtj
  1

• merging bgt files split by chromosome into one

  #10 opened 8 years ago by pontikos
  1

• getting private variants from an individual

  #9 opened 8 years ago by pontikos
  1

• Unable to find insertions

  #5 opened 9 years ago by zacdanielson
  2

• freebayes vcfs (1.0-r282 and 1.0-r265)

  #6 opened 9 years ago by ml4wc
  7

• Server addresses in the example

  #4 opened 9 years ago by zhanxw
  1

• Tests

  #3 opened 9 years ago by ekg
  2

• Handling large annotation sets

  #2 opened 9 years ago by ekg
  2

• compilation issue

  #1 opened 10 years ago by mcshane
  2