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Comment: Comment: segmentation fault in Bayenv2
2.5 years ago by QPaps04 ▴ 140
0
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1
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4.2k
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Comment: Comment: segmentation fault in Bayenv2
2.5 years ago by QPaps04 ▴ 140
0
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0
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4.2k
views
Comment: Comment: segmentation fault in Bayenv2
2.5 years ago by QPaps04 ▴ 140
0
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0
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1.6k
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Comment: Comment: bayenv2: "initial epsilon zero or 1 locus 6912"
2.5 years ago by QPaps04 ▴ 140
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1
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1.1k
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Comment: Comment: individual-level allele frequencies
2.7 years ago by QPaps04 ▴ 140
0
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0
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24k
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Comment: Comment: LD-decay in a r2 vs distance(cm) plot
2.9 years ago by QPaps04 ▴ 140
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0
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1.1k
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Comment: Comment: Convert phased vcf to Chromosome/scaffold + Tag Haplotype Matrix
3.0 years ago by QPaps04 ▴ 140
0
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1
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1.1k
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Comment: Comment: Convert phased vcf to Chromosome/scaffold + Tag Haplotype Matrix
3.0 years ago by QPaps04 ▴ 140
0
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4
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1.1k
views
Convert phased vcf to Chromosome/scaffold + Tag Haplotype Matrix
vcf phased haplotypes shapeit bcftools
3.0 years ago by QPaps04 ▴ 140
0
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0
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7.2k
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Comment: C: How to parallelize bcftools mpileup with GNU parallel?
3.2 years ago by QPaps04 ▴ 140
0
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0
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1.8k
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Filter max-missing multiple time removes more SNPs
SNP filtering vcftools linux sequencing
3.4 years ago by QPaps04 ▴ 140
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0
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3.3k
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Comment: C: Alternative to PGDSpider for vcf conversion
3.4 years ago by QPaps04 ▴ 140
1
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3
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3.3k
views
Alternative to PGDSpider for vcf conversion
vcf SNP next-gen conversion memory
updated 3.6 years ago by • 0 • written 3.9 years ago by ▴ 140
0
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0
replies
818
views
Deeptools plotCoverage and bamPEFragmentSize change axes
Deeptools coverage sequencing snp next-gen
3.6 years ago by QPaps04 ▴ 140
6
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2
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6.9k
views
Answer: Answer: VCFTools error: Unrecognized values used for CHROM, Replacing with 0.
updated 2.4 years ago by 43k • written 3.6 years ago by ▴ 140
8
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2
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2.7k
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remove listed singletons from vcftools output
vcftools sequencing genome next-gen
updated 9 months ago by • 0 • written 4.0 years ago by ▴ 140
6
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1
reply
2.7k
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Answer: A: remove listed singletons from vcftools output
4.0 years ago by QPaps04 ▴ 140
0
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0
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1.1k
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Comment: C: Filter SNPs for DP using mean + 2*SD
4.0 years ago by QPaps04 ▴ 140
0
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1
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1.1k
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Comment: C: Filter SNPs for DP using mean + 2*SD
4.0 years ago by QPaps04 ▴ 140
0
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3
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1.1k
views
Filter SNPs for DP using mean + 2*SD
SNP next-gen Filter depth vcftools
4.0 years ago by QPaps04 ▴ 140
0
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0
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3.2k
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Comment: C: how to estimate mean and standard deviation read depth for all the variants?
4.0 years ago by QPaps04 ▴ 140
0
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0
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1.2k
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Comment: A: Filter SNPs in multiple-sample vcf based on the snps of two samples
4.2 years ago by QPaps04 ▴ 140
0
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3
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1.2k
views
Filter SNPs in multiple-sample vcf based on the snps of two samples
vcf SNP filter bash linux
4.2 years ago by QPaps04 ▴ 140
0
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0
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4.5k
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Comment: C: comparing vcf files of disease and normal samples
4.2 years ago by QPaps04 ▴ 140
0
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1
reply
11k
views
Comment: C: bwa for multiple fastq files
4.9 years ago by QPaps04 ▴ 140
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