Difference between revisions of "2017 Haneul Lab note"

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(Mungbean synchronous QTL)
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== 1/9 ==
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== 1 / 9 ==
 
=== Minyoung_UV_QTL ===
 
=== Minyoung_UV_QTL ===
 
  parsing genotype data(Joinmap) and phenotype data to ICImapping format(bip format)
 
  parsing genotype data(Joinmap) and phenotype data to ICImapping format(bip format)
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=== 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/)
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== 1 / 10 ==
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=== Minyoung_UV_QTL ===
 +
 +
=== Mungbean synchronous QTL ===
 +
 +
=== Mungbean pacbio assembly ===
 +
convert SAM format to BAM format (244:/kev8305/SK3/convertbam.sh)

Revision as of 01:23, 10 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 grouping 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/)

1 / 10

Minyoung_UV_QTL

Mungbean synchronous QTL

Mungbean pacbio assembly

convert SAM format to BAM format (244:/kev8305/SK3/convertbam.sh)