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Comment: Comment: segmentation fault in Bayenv2
3.3 years ago by QPaps04 ▴ 160
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1
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5.0k
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Comment: Comment: segmentation fault in Bayenv2
3.3 years ago by QPaps04 ▴ 160
0
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0
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5.0k
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Comment: Comment: segmentation fault in Bayenv2
3.3 years ago by QPaps04 ▴ 160
0
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0
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1.8k
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Comment: Comment: bayenv2: "initial epsilon zero or 1 locus 6912"
3.3 years ago by QPaps04 ▴ 160
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1
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1.3k
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Comment: Comment: individual-level allele frequencies
3.5 years ago by QPaps04 ▴ 160
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0
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27k
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Comment: Comment: LD-decay in a r2 vs distance(cm) plot
3.7 years ago by QPaps04 ▴ 160
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0
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1.4k
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Comment: Comment: Convert phased vcf to Chromosome/scaffold + Tag Haplotype Matrix
3.8 years ago by QPaps04 ▴ 160
0
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1
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1.4k
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Comment: Comment: Convert phased vcf to Chromosome/scaffold + Tag Haplotype Matrix
3.8 years ago by QPaps04 ▴ 160
0
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4
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1.4k
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Convert phased vcf to Chromosome/scaffold + Tag Haplotype Matrix
vcf phased haplotypes shapeit bcftools
3.8 years ago by QPaps04 ▴ 160
0
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0
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8.3k
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Comment: C: How to parallelize bcftools mpileup with GNU parallel?
4.0 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
4.2 years ago by QPaps04 ▴ 160
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3.9k
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Comment: C: Alternative to PGDSpider for vcf conversion
4.2 years ago by QPaps04 ▴ 160
1
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3
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3.9k
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Alternative to PGDSpider for vcf conversion
vcf SNP next-gen conversion memory
updated 4.4 years ago by • 0 • written 4.7 years ago by ▴ 160
0
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0
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967
views
Deeptools plotCoverage and bamPEFragmentSize change axes
Deeptools coverage sequencing snp next-gen
4.4 years ago by QPaps04 ▴ 160
7
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2
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7.7k
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Answer: Answer: VCFTools error: Unrecognized values used for CHROM, Replacing with 0.
updated 3.2 years ago by 44k • written 4.5 years ago by ▴ 160
9
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2
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3.2k
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remove listed singletons from vcftools output
vcftools sequencing genome next-gen
updated 19 months ago by • 0 • written 4.8 years ago by ▴ 160
7
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1
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3.2k
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Answer: A: remove listed singletons from vcftools output
4.8 years ago by QPaps04 ▴ 160
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0
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1.3k
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Comment: C: Filter SNPs for DP using mean + 2*SD
4.8 years ago by QPaps04 ▴ 160
0
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1
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1.3k
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Comment: C: Filter SNPs for DP using mean + 2*SD
4.8 years ago by QPaps04 ▴ 160
0
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3
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1.3k
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Filter SNPs for DP using mean + 2*SD
SNP next-gen Filter depth vcftools
4.8 years ago by QPaps04 ▴ 160
0
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0
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3.5k
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Comment: C: how to estimate mean and standard deviation read depth for all the variants?
4.8 years ago by QPaps04 ▴ 160
0
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3
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1.4k
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Filter SNPs in multiple-sample vcf based on the snps of two samples
vcf SNP filter bash linux
5.0 years ago by QPaps04 ▴ 160
0
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0
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1.4k
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Comment: A: Filter SNPs in multiple-sample vcf based on the snps of two samples
5.0 years ago by QPaps04 ▴ 160
0
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0
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4.8k
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Comment: C: comparing vcf files of disease and normal samples
5.1 years ago by QPaps04 ▴ 160
0
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1
reply
12k
views
Comment: C: bwa for multiple fastq files
5.7 years ago by QPaps04 ▴ 160
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