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Answer: Answer: gnomAD4.0 Hail Table Downloading
6 weeks ago by DBScan ▴ 300
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985
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Answer: Answer: Nextflow and self-made pipelines opinion
8 weeks ago by DBScan ▴ 300
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436
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Answer: Answer: how to extract variants from the vcf.gz files linked below?
9 weeks ago by DBScan ▴ 300
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412
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Answer: Answer: What is the best GWAS tool to use for a very large cohort data (UK Biobank data)
11 weeks ago by DBScan ▴ 300
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588
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Answer: Answer: fill-from-fasta doesnt fill missing values in REF
3 months ago by DBScan ▴ 300
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548
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Answer: Answer: Suggestions for a simpler solution for collecting snakemake rule output in a tex
3 months ago by DBScan ▴ 300
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704
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Answer: Answer: Problem with DRAGEN RNAseq hashtable directory
3 months ago by DBScan ▴ 300
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350
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Answer: Answer: how to merge two files without duplicating same column
3 months ago by DBScan ▴ 300
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857
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Answer: Answer: Snakemake alignment script
7 months ago by DBScan ▴ 300
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505
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Answer: Answer: VCF QUAL field for multiple samples
7 months ago by DBScan ▴ 300
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698
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Answer: Answer: BWA-mem2 vs Bowtie2: no deterministic option
8 months ago by DBScan ▴ 300
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1.2k
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Answer: Answer: T2T fixed GRCg38 gaps and issues, gaps genomic coordinates.
8 months ago by DBScan ▴ 300
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754
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Answer: Answer: vcf file
8 months ago by DBScan ▴ 300
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1.6k
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Answer: Answer: The result of Illumina/hap.py using the same file.
8 months ago by DBScan ▴ 300
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1.3k
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Answer: Answer: How to liftover SNP positions from one genome to another genome?
9 months ago by DBScan ▴ 300
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749
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Answer: Answer: bcftools view to failed reader data
9 months ago by DBScan ▴ 300
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3.0k
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Answer: Answer: Conda/Mamba environment activation error
9 months ago by DBScan ▴ 300
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1.1k
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Answer: Answer: Rstudio server in Snakemake
9 months ago by DBScan ▴ 300
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497
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Answer: Answer: BWA MEM -K option
9 months ago by DBScan ▴ 300
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690
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Answer: Answer: strelka variant calling
9 months ago by DBScan ▴ 300
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2.1k
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Answer: Answer: KING kinship inference error
11 months ago by DBScan ▴ 300
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1.3k
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Answer: Answer: How to efficiently/quickly merge ~500k vcfs?
11 months ago by DBScan ▴ 300
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543
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Answer: Answer: Why is NA18498 sample missing from 1000 genome GRCh38 vcf file?
12 months ago by DBScan ▴ 300
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429
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Answer: Answer: Tools for super-enhancers prediction
17 months ago by DBScan ▴ 300
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647
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Answer: A: how to understand taking a derivative in using MLE?
3.5 years ago by DBScan ▴ 300
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2.4k
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Answer: A: Deeptools installation fails (Could not find a version that satisfies the requir
3.6 years ago by DBScan ▴ 300
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2.2k
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Answer: A: GSVA on enrichment scores about R project
3.7 years ago by DBScan ▴ 300
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3
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3.1k
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Answer: A: Getting error while installing other packages in R after installing Rtools40 pac
3.8 years ago by DBScan ▴ 300
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