Difference between revisions of "2017 Haneul Lab note"
From Crop Genomics Lab.
(→Mungbean synchronous QTL) |
(→Mungbean synchronous QTL) |
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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 | + | while grouping 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 09:41, 9 January 2017
Contents |
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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/)