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Comment: Comment: segmentation fault in Bayenv2
3.6 years ago by QPaps04 ▴ 160
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1
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5.5k
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Comment: Comment: segmentation fault in Bayenv2
3.6 years ago by QPaps04 ▴ 160
0
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0
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5.5k
views
Comment: Comment: segmentation fault in Bayenv2
3.6 years ago by QPaps04 ▴ 160
0
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0
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2.0k
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Comment: Comment: bayenv2: "initial epsilon zero or 1 locus 6912"
3.6 years ago by QPaps04 ▴ 160
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1
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1.4k
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Comment: Comment: individual-level allele frequencies
3.9 years ago by QPaps04 ▴ 160
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28k
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Comment: Comment: LD-decay in a r2 vs distance(cm) plot
4.0 years ago by QPaps04 ▴ 160
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0
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1.5k
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Comment: Comment: Convert phased vcf to Chromosome/scaffold + Tag Haplotype Matrix
4.1 years ago by QPaps04 ▴ 160
0
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1
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1.5k
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Comment: Comment: Convert phased vcf to Chromosome/scaffold + Tag Haplotype Matrix
4.1 years ago by QPaps04 ▴ 160
0
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4
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1.5k
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Convert phased vcf to Chromosome/scaffold + Tag Haplotype Matrix
vcf phased haplotypes shapeit bcftools
4.1 years ago by QPaps04 ▴ 160
0
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0
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9.0k
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Comment: C: How to parallelize bcftools mpileup with GNU parallel?
4.3 years ago by QPaps04 ▴ 160
0
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0
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2.0k
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Filter max-missing multiple time removes more SNPs
SNP filtering vcftools linux sequencing
4.5 years ago by QPaps04 ▴ 160
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4.2k
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Comment: C: Alternative to PGDSpider for vcf conversion
4.5 years ago by QPaps04 ▴ 160
1
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3
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4.2k
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Alternative to PGDSpider for vcf conversion
vcf SNP next-gen conversion memory
updated 4.7 years ago by • 0 • written 5.1 years ago by ▴ 160
0
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0
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1.0k
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Deeptools plotCoverage and bamPEFragmentSize change axes
Deeptools coverage sequencing snp next-gen
4.8 years ago by QPaps04 ▴ 160
7
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2
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8.0k
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Answer: Answer: VCFTools error: Unrecognized values used for CHROM, Replacing with 0.
updated 3.5 years ago by 45k • written 4.8 years ago by ▴ 160
7
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1
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3.4k
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Answer: A: remove listed singletons from vcftools output
5.1 years ago by QPaps04 ▴ 160
9
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2
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3.4k
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remove listed singletons from vcftools output
vcftools sequencing genome next-gen
updated 23 months ago by • 0 • written 5.1 years ago by ▴ 160
0
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0
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1.4k
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Comment: C: Filter SNPs for DP using mean + 2*SD
5.2 years ago by QPaps04 ▴ 160
0
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1
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1.4k
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Comment: C: Filter SNPs for DP using mean + 2*SD
5.2 years ago by QPaps04 ▴ 160
0
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3
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1.4k
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Filter SNPs for DP using mean + 2*SD
SNP next-gen Filter depth vcftools
5.2 years ago by QPaps04 ▴ 160
0
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0
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3.6k
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Comment: C: how to estimate mean and standard deviation read depth for all the variants?
5.2 years ago by QPaps04 ▴ 160
0
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0
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1.5k
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Comment: A: Filter SNPs in multiple-sample vcf based on the snps of two samples
5.4 years ago by QPaps04 ▴ 160
0
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3
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1.5k
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Filter SNPs in multiple-sample vcf based on the snps of two samples
vcf SNP filter bash linux
5.4 years ago by QPaps04 ▴ 160
0
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0
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5.0k
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Comment: C: comparing vcf files of disease and normal samples
5.4 years ago by QPaps04 ▴ 160
0
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1
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12k
views
Comment: C: bwa for multiple fastq files
6.1 years ago by QPaps04 ▴ 160
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