Difference between revisions of "2017 Haneul Lab note"
From Crop Genomics Lab.
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=== 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 == | ||
+ | === Minyoung_UV_QTL === | ||
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+ | === Mungbean synchronous QTL === | ||
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+ | === 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)