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Answer: A: Multiple testing correction in linear mixed models (MLM) for GWAS
5.7 years ago by pfs ▴ 280
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Answer: A: Where can I find the info about the start/end position of sets of SNP's that are
6.2 years ago by pfs ▴ 280
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Answer: A: how to combain microarray sets from the same platform but raw data were normaliz
6.3 years ago by pfs ▴ 280
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Answer: A: Regenotype vcf using some samples as reference
6.3 years ago by pfs ▴ 280
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Answer: A: finding function of genes from their coordinates
6.3 years ago by pfs ▴ 280
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Answer: A: Suggestions regarding bioinformatics journal
6.4 years ago by pfs ▴ 280
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Answer: A: SNPSVM - not able to find VCF file
6.4 years ago by pfs ▴ 280
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Answer: A: Given QTLs and genome annotation, quickly list genes closest to QTLs
6.4 years ago by pfs ▴ 280
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1.3k
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Answer: A: SNPSVM - not able to find VCF file
6.4 years ago by pfs ▴ 280
4
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2.2k
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Answer: A: SNP calling from a scaffold.fa file
6.4 years ago by pfs ▴ 280
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4.5k
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Answer: A: value too large for defined data type using bgzip
6.4 years ago by pfs ▴ 280
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Answer: A: (Sanity check) Too many SNPs?
6.5 years ago by pfs ▴ 280
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Answer: A: Finding GO terms for an organism not in a GO database
6.5 years ago by pfs ▴ 280
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1.7k
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Answer: A: Conditional analysis on dosage file -what program to use?
6.5 years ago by pfs ▴ 280
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6.5k
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Answer: A: How to make variant calling run faster?
6.5 years ago by pfs ▴ 280
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Answer: A: Compare between two columns of two different files and print common
6.5 years ago by pfs ▴ 280
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5.8k
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Answer: A: Compare between two columns of two different files and print common
6.5 years ago by pfs ▴ 280
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Answer: A: difference between 2 snp's data annotations
6.5 years ago by pfs ▴ 280
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Answer: A: How to find the unique list of mismatches of reads with the reference genome
6.5 years ago by pfs ▴ 280
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3.0k
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Answer: A: Reference and mutant allele of a SNP rsID
6.6 years ago by pfs ▴ 280
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1.5k
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Answer: A: Indentical proteins but different Blast results
6.6 years ago by pfs ▴ 280
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3.4k
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Answer: A: Subsetting individuals in PLINK when IDs contain underscores "_"
6.6 years ago by pfs ▴ 280
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5.4k
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Answer: A: Using Plink, get allele frequencies for a subset of individuals
6.6 years ago by pfs ▴ 280
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9.9k
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Answer: A: plink calculating LD using R2 command
6.6 years ago by pfs ▴ 280
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1.7k
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Answer: A: Recode SNPs dataset to Number
6.6 years ago by pfs ▴ 280
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2.0k
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Answer: A: VCF mining & interpretation tools (hg38 build)
6.6 years ago by pfs ▴ 280
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2.0k
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Answer: A: VCF mining & interpretation tools (hg38 build)
6.6 years ago by pfs ▴ 280
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2.8k
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Answer: A: HaplotypeCaller filter out variants covered only in one direction
6.7 years ago by pfs ▴ 280
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2.6k
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Answer: A: Any great tutorials on how to download sift/provean on your computer?
6.7 years ago by pfs ▴ 280
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