Difference between revisions of "2017 Haneul Lab note"
From Crop Genomics Lab.
Line 61: | Line 61: | ||
make svg file for superscaffold - linkage group marker location (63:/home/skyts0401/svg/) | make svg file for superscaffold - linkage group marker location (63:/home/skyts0401/svg/) | ||
python make_chr_lg_svg.py standard_output.final.scaffolds.fasta.tr.JM_out.fa standard_output.final.scaffolds.fasta LG.total.txt.reformed standard_output.final.scaffolds.fasta.tr.JM_out.fa.log > chr_lg.svg | python make_chr_lg_svg.py standard_output.final.scaffolds.fasta.tr.JM_out.fa standard_output.final.scaffolds.fasta LG.total.txt.reformed standard_output.final.scaffolds.fasta.tr.JM_out.fa.log > chr_lg.svg | ||
+ | |||
+ | == 1/31 == | ||
+ | === Mungbean Chloroplast assembly === | ||
+ | pairing Illumina PE read (63:/home/skyts0401/) | ||
+ | sudo python PE-pairing.py /data/jungminh/mungbean/PE/SunhwaN_1_cont.fq /data/jungminh/mungbean/PE/SunhwaN_2_cont.fq |
Revision as of 01:45, 1 February 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
QTL analysis by using IciMapping
Mungbean synchronous QTL
construct genetic map (JoinMap 4.1), just using chr 3, 4 combined and chr 5 splited linkage group.
ML method, Haldane algorithm
Mungbean pacbio assembly
convert SAM format to BAM format (244:/kev8305/SK3/)
./convertbam.sh
1/ 11
Mungbean synchronous QTL
QTL analysis by using RQTL(desktop:/Users/sky/desktop/Mungbean_syn_RQTL.csv) just for checking locus
1/16
Mungbean pacbio assembly
coping sorted.bam file from 244 server to 63 server
variant calling (244:/kev8305/SK3/, 63:/data/skyts0401/Mungbean/mapping/resequencing/)
samtools mpileup -f falcon_500_sspace.final.scaffolds.fasta -v -t DP,AD,ADF,ADR,SP,INFO/AD,INFO/ADF,INFO/ADR -b bam_list | bcftools call -v -m -O v > variants.vcf samtools mpileup -f falcon_500_sspace.final.scaffolds.fasta -I -v -t DP,AD,ADF,ADR,SP,INFO/AD,INFO/ADF,INFO/ADR -b bam_list | bcftools call -v -m -O v > variants_snp.vcf
1/18
Mungbean pacbio assembly
variant calling Kyoungki Jarae #5 with pacbio falcon scaffold (63:/data/skyts0401/Mungbean/mapping/resequencing/)
bwa index falcon_500_sspace.final.scaffolds.fasta bwa mem -t 10 falcon_500_sspace.final.scaffolds.fasta KJ-C_1.fastq.gz KJ-C_2.fastq.gz > KJ-pe_falcon_scaffold.sam
1/19
Mungbean pacbio assembly
variant calling Kyoungki Jarae #5 with pacbio falcon scaffold (63:/data/skyts0401/Mungbean/mapping/resequencing/)
samtools view -Sb KJ-pe_falcon_scaffold.sam > KJ-pe_falcon_scaffold.bam samtools sort KJ-pe_falcon_scaffold.bam -o KJ-pe_falcon_scaffold.sorted.bam samtools index KJ-pe_falcon_scaffold.sorted.bam samtools mpileup -f falcon_500_sspace.final.scaffolds.fasta -I -v -t DP,AD,ADF,ADR,SP,INFO/AD,INFO/ADF,INFO/ADR -u KJ-pe_falcon_scaffold.sorted.bam | bcftools call -v -m -O v > KJ_falcon_scaffold_variants_snp.vcf
1/24
Jatropha assembly
make svg file for superscaffold - linkage group marker location (63:/home/skyts0401/svg/)
python make_chr_lg_svg.py standard_output.final.scaffolds.fasta.tr.JM_out.fa standard_output.final.scaffolds.fasta LG.total.txt.reformed standard_output.final.scaffolds.fasta.tr.JM_out.fa.log > chr_lg.svg
1/31
Mungbean Chloroplast assembly
pairing Illumina PE read (63:/home/skyts0401/)
sudo python PE-pairing.py /data/jungminh/mungbean/PE/SunhwaN_1_cont.fq /data/jungminh/mungbean/PE/SunhwaN_2_cont.fq