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selplat21
selplat21
Reputation:
20 (New)
Joined:
7.4 years ago
Last seen:
2.0 years ago
Location:
United States
Latest posts by user
0 votes
0 replies
646 views
Merging Imputed VCF with Reference Panel VCF
vcf glimpse imputation
written by selplat21 2
0 votes
0 replies
0 views
Comment: Comment: Plotting LD heat map with plink.ld result
written by selplat21 2
0 votes
2 replies
2.3K views
Plotting LD heat map with plink.ld result
r
written by selplat21 2
0 votes
1 reply
0 views
Comment: Comment: Header too long for bam format
written by selplat21 2
0 votes
3 replies
2.1K views
Header too long for bam format
samtools alignments
updated by Ram 4.5K • | written by selplat21 2
0 votes
0 replies
0 views
Comment: Comment: Download data from data dryad using CLI?
written by selplat21 2
0 votes
3 replies
2.0K views
Download data from data dryad using CLI?
datadryad
written by selplat21 2
0 votes
1 reply
0 views
Comment: Comment: Bcftools consensus unexpected output
written by selplat21 2
0 votes
3 replies
907 views
Bcftools consensus unexpected output
bcftools
updated by Ram 4.5K • | written by selplat21 2
0 votes
0 replies
732 views
Bcftools consensus when reference is a deletion
consensus vcf
written by selplat21 2
0 votes
0 replies
697 views
Bcftools Consensus - Choose Random Allele for Heterozygous Sites
bcftools
updated by Ram 4.5K • | written by selplat21 2
0 votes
0 replies
711 views
Sample based on allele frequency matching between two files
linkage
updated by Ram 4.5K • | written by selplat21 2
0 votes
0 replies
0 views
Comment: Comment: Transform TSV file
written by selplat21 2
0 votes
0 replies
0 views
Comment: Comment: Removing or Setting pairs to NA based on conditions in another data frame (R)
written by selplat21 2
0 votes
2 replies
1.2K views
Removing or Setting pairs to NA based on conditions in another data frame (R)
r
written by selplat21 2
0 votes
0 replies
0 views
Comment: Comment: Set random genotypes to missing in VCF file by individuals and sites
written by selplat21 2
1 vote
0 replies
0 views
Answer: Answer: Convert rows to columns delimited by each SNP ID
updated by GenoMax 16K • | written by selplat21 2
0 votes
2 replies
1.4K views
Set random genotypes to missing in VCF file by individuals and sites
imputation
written by selplat21 2
0 votes
0 replies
0 views
Comment: Comment: Convert rows to columns delimited by each SNP ID
written by selplat21 2
0 votes
0 replies
0 views
Comment: Comment: Convert rows to columns delimited by each SNP ID
written by selplat21 2
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