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581
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Historical Genbank genome assemblies missing?
genome Assembly
updated 3.8 years ago by 147k • written 3.8 years ago by ▴ 80
0
votes
0
replies
503
views
Synteny map files for human and mouse for GRCh37
genome
3.9 years ago by Tails ▴ 80
0
votes
3
replies
927
views
Need help finding data from Google's DeepVariant paper
genome snp sequencing
updated 4.6 years ago by 20 • written 4.8 years ago by ▴ 80
1
vote
1
reply
2.3k
views
Comment: C: Benchmarking small variant calls: TP, FP, TN, FN
4.7 years ago by Tails ▴ 80
3
votes
3
replies
1.3k
views
Can a command in RTG (or elsewhere) annotate the TP/TN/FP/FN's produced from RTG's vcfeval?
sequence genome
updated 4.8 years ago by ★ 1.6k • written 4.8 years ago by ▴ 80
0
votes
1
reply
1.4k
views
Comment: C: Correct reference for Platinum Genomes?
4.8 years ago by Tails ▴ 80
0
votes
1
reply
1.4k
views
Comment: C: Correct reference for Platinum Genomes?
4.8 years ago by Tails ▴ 80
1
vote
5
replies
1.4k
views
Correct reference for Platinum Genomes?
genome sequencing
updated 17 months ago by 44k • written 4.8 years ago by ▴ 80
0
votes
1
reply
927
views
Comment: C: Need help finding data from Google's DeepVariant paper
4.8 years ago by Tails ▴ 80
0
votes
0
replies
3.7k
views
Comment: C: How to filter GTF file and only print lines where the tag is a certain value?
5.2 years ago by Tails ▴ 80
0
votes
2
replies
3.7k
views
Comment: C: How to filter GTF file and only print lines where the tag is a certain value?
5.2 years ago by Tails ▴ 80
1
vote
8
replies
3.7k
views
How to filter GTF file and only print lines where the tag is a certain value?
GTF awk
5.2 years ago by Tails ▴ 80
0
votes
1
reply
3.7k
views
Comment: C: How to filter GTF file and only print lines where the tag is a certain value?
5.2 years ago by Tails ▴ 80
24
votes
9
replies
26k
views
10 follow
Variant call format (VCF) file, how to get statistics per sample?
vcf
updated 19 months ago by ▴ 740 • written 9.3 years ago by ▴ 80
6
votes
4
replies
2.3k
views
Benchmarking small variant calls: TP, FP, TN, FN
genome sequencing SNP
updated 5.5 years ago by 47k • written 5.5 years ago by ▴ 80
0
votes
1
reply
1.0k
views
Best resources for understanding GATK best practices pipeline (or similar)
Assembly sequence alignment genome snp
updated 5.5 years ago by 88k • written 5.5 years ago by ▴ 80
0
votes
2
replies
5.2k
views
How to extract entire info column from VCF file using bcftools
bcftools software error SNP
updated 5.6 years ago by 16k • written 5.6 years ago by ▴ 80
0
votes
0
replies
3.4k
views
Beagle imputation output, incorrect genotype probability format?
BEAGLE imputation sequence
updated 23 months ago by 44k • written 9.5 years ago by ▴ 80
7
votes
1
reply
3.7k
views
How to get GQ after running BCFTools?
sequencing SNP
updated 9.7 years ago by ▴ 50 • written 9.9 years ago by ▴ 80
2
votes
1
reply
1.4k
views
Missing -d option in new BCFTools?
sequence SNP
updated 9.9 years ago by 44k • written 9.9 years ago by ▴ 80
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