Difference between revisions of "2017 Haneul Lab note"

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(Minyoung_UV_QTL)
(Mungbean synchronous QTL)
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=== Mungbean synchronous QTL ===
 
=== Mungbean synchronous QTL ===
 
  make loc file(244:/home/skyts0401/reseq/chr/Mungbean_chr_coseq_parse_seg_dist.loc)
 
  make loc file(244:/home/skyts0401/reseq/chr/Mungbean_chr_coseq_parse_seg_dist.loc)
 
 
  missing > 10%, hetero > 10, depth < 3 marker is filtered
 
  missing > 10%, hetero > 10, depth < 3 marker is filtered
 
 
  while groupings them, find vr03, vr04 is combined in a group and vr05 is splited 2 groups, check it.
 
  while groupings them, find vr03, vr04 is combined in a group and vr05 is splited 2 groups, check it.
  
 
=== Mungbean pacbio assembly ===
 
=== Mungbean pacbio assembly ===
 
  moving SAM data(align reseq data on pacbio-scaffold) from NICEM server to 244 server (244:/kev8305/SK3/)
 
  moving SAM data(align reseq data on pacbio-scaffold) from NICEM server to 244 server (244:/kev8305/SK3/)

Revision as of 09:40, 9 January 2017

Contents

1/9

Minyoung_UV_QTL

parsing genotype data(Joinmap) and phenotype data to ICImapping format(bip format)
using lgcombine.py(63:/data/skyts0401/Mungbean/MY_UV/)
find linkage group 2 map is wrong, construct map newly

Mungbean synchronous QTL

make loc file(244:/home/skyts0401/reseq/chr/Mungbean_chr_coseq_parse_seg_dist.loc)
missing > 10%, hetero > 10, depth < 3 marker is filtered
while groupings them, find vr03, vr04 is combined in a group and vr05 is splited 2 groups, check it.

Mungbean pacbio assembly

moving SAM data(align reseq data on pacbio-scaffold) from NICEM server to 244 server (244:/kev8305/SK3/)