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Tails
Tails
Reputation:
80
Joined:
11.6 years ago
Last seen:
5.2 years ago
Location:
New Zealand
Latest posts by user
0 votes
1 reply
847 views
Historical Genbank genome assemblies missing?
genome assembly
updated by GenoMax GenoMax • written by Tails Tails
0 votes
0 replies
687 views
Synteny map files for human and mouse for GRCh37
genome
written by Tails Tails
1 vote
1 reply
0 views
Comment: C: Benchmarking small variant calls: TP, FP, TN, FN
written by Tails Tails
0 votes
1 reply
0 views
Comment: C: Correct reference for Platinum Genomes?
written by Tails Tails
0 votes
1 reply
0 views
Comment: C: Correct reference for Platinum Genomes?
written by Tails Tails
0 votes
5 replies
2.0K views
Correct reference for Platinum Genomes?
genome sequencing
updated by Ram Ram • written by Tails Tails
1 vote
3 replies
1.9K views
Can a command in RTG (or elsewhere) annotate the TP/TN/FP/FN's produced from RTG's vcfeval?
sequence genome
updated by Len Trigg Len Trigg • written by Tails Tails
0 votes
1 reply
0 views
Comment: C: Need help finding data from Google's DeepVariant paper
written by Tails Tails
0 votes
3 replies
1.5K views
Need help finding data from Google's DeepVariant paper
genome snp sequencing
updated by Biostar Biostar • written by Tails Tails
0 votes
0 replies
0 views
Comment: C: How to filter GTF file and only print lines where the tag is a certain value?
written by Tails Tails
0 votes
2 replies
0 views
Comment: C: How to filter GTF file and only print lines where the tag is a certain value?
written by Tails Tails
0 votes
1 reply
0 views
Comment: C: How to filter GTF file and only print lines where the tag is a certain value?
written by Tails Tails
0 votes
8 replies
4.8K views
How to filter GTF file and only print lines where the tag is a certain value?
gtf awk
written by Tails Tails
1 vote
4 replies
3.2K views
Benchmarking small variant calls: TP, FP, TN, FN
genome sequencing snp
updated by WouterDeCoster WouterDeCoster • written by Tails Tails
0 votes
1 reply
1.7K views
Best resources for understanding GATK best practices pipeline (or similar)
assembly sequence alignment genome snp
updated by Kevin Blighe Kevin Blighe • written by Tails Tails
0 votes
2 replies
6.2K views
How to extract entire info column from VCF file using bcftools
bcftools software error snp
updated by finswimmer finswimmer • written by Tails Tails
3 votes
9 replies
28K views
Variant call format (VCF) file, how to get statistics per sample?
vcf
updated by O.rka O.rka • written by Tails Tails
0 votes
0 replies
3.7K views
Beagle imputation output, incorrect genotype probability format?
beagle imputation sequence
updated by Ram Ram • written by Tails Tails
0 votes
1 reply
1.6K views
Missing -d option in new BCFTools?
sequence snp
updated by Ram Ram • written by Tails Tails
2 votes
1 reply
4.3K views
How to get GQ after running BCFTools?
sequencing snp
updated by timothee.cezard • timothee.cezard • written by Tails Tails
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