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2
votes
1
reply
12k
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Answer:
Answer: Parabricks : Number of GPUs requested (2) is more than number of GPUs (0) in the
10 days ago by
DBScan
▴ 530
6
votes
1
reply
818
views
hg38 vs GRCh38 chr prefix
human
genome
reference
updated 8 weeks ago by
GenoMax
153k • written 8 weeks ago by
DBScan
▴ 530
1
vote
0
replies
700
views
Answer:
Answer: Joint Calling for Large Germline WGS Cohort
10 weeks ago by
DBScan
▴ 530
1
vote
0
replies
573
views
Answer:
Answer: Error running pbrun fq2bam: No space left on device
11 weeks ago by
DBScan
▴ 530
0
votes
0
replies
5.6k
views
Answer:
Answer: bcftools query add header
4 months ago by
DBScan
▴ 530
0
votes
1
reply
1.1k
views
Comment:
Comment: DRAGEN FILTER
4 months ago by
DBScan
▴ 530
1
vote
0
replies
594
views
Comment:
Comment: Using Principal Components may muddle the detecting power of a GWAS?
5 months ago by
DBScan
▴ 530
0
votes
1
reply
773
views
Comment:
Comment: Snakemake Global Environment Container
5 months ago by
DBScan
▴ 530
0
votes
1
reply
773
views
Comment:
Comment: Snakemake Global Environment Container
5 months ago by
DBScan
▴ 530
0
votes
1
reply
395
views
Fast querying of variant metrics with database
python
database
updated 6 months ago by
Pierre Lindenbaum
166k • written 6 months ago by
DBScan
▴ 530
2
votes
0
replies
915
views
Answer:
Answer: Snakemake version 8.27.1 on LSF cluster
7 months ago by
DBScan
▴ 530
0
votes
0
replies
944
views
Comment:
Comment: Giraffe DeepVariant workflow
10 months ago by
DBScan
▴ 530
2
votes
2
replies
944
views
Giraffe DeepVariant workflow
deepvariant
vg
giraffe
updated 10 months ago by
Istvan Albert
103k • written 10 months ago by
DBScan
▴ 530
0
votes
1
reply
953
views
Comment:
Comment: bcftools/vt split multiallelics - split GT along with splitting multi-allelics
11 months ago by
DBScan
▴ 530
1
vote
1
reply
3.4k
views
Answer:
Answer: RNA-Seq mutation calling without germline data
11 months ago by
DBScan
▴ 530
0
votes
0
replies
965
views
Answer:
Answer: Removing conda environment created in a snakemake workflow
11 months ago by
DBScan
▴ 530
2
votes
0
replies
1.4k
views
Answer:
Answer: Ancestry estimation using 1000 genomes as reference
12 months ago by
DBScan
▴ 530
3
votes
0
replies
1.7k
views
Answer:
Answer: are illumina fastq files typically split by lane?
13 months ago by
DBScan
▴ 530
1
vote
1
reply
1.0k
views
Comment:
Comment: How to fix this error while performing QC in PLINK "Warning: 228 het. haploid g
13 months ago by
DBScan
▴ 530
3
votes
1
reply
1.4k
views
Answer:
Answer: Seeking Advice on Multisample Variant Calling Pipeline with BWA-MEME and GATK DR
14 months ago by
DBScan
▴ 530
1
vote
0
replies
840
views
Answer:
Answer: batchtools_slurm job setting with seurat
14 months ago by
DBScan
▴ 530
0
votes
0
replies
2.5k
views
Answer:
Answer: looking for 1000g hg38 reference data to anchor with my genomic data to plot th
14 months ago by
DBScan
▴ 530
2
votes
3
replies
910
views
Snakemake rule to copy files
snakemake
updated 14 months ago by
raphael.B
▴ 540 • written 14 months ago by
DBScan
▴ 530
2
votes
0
replies
910
views
Answer:
Answer: Snakemake rule to copy files
14 months ago by
DBScan
▴ 530
0
votes
1
reply
756
views
Answer:
Answer: Add tags/ header lines to a vcf file
15 months ago by
DBScan
▴ 530
0
votes
1
reply
1.7k
views
Comment:
Comment: Asking for parallel jobs setting on HPC when analyzing sequencing data
15 months ago by
DBScan
▴ 530
2
votes
1
reply
1.7k
views
Comment:
Comment: Asking for parallel jobs setting on HPC when analyzing sequencing data
15 months ago by
DBScan
▴ 530
1
vote
1
reply
1.6k
views
Comment:
Comment: How to get the ratio of allele counts from GATK derived VCF file?
16 months ago by
DBScan
▴ 530
0
votes
0
replies
721
views
Comment:
Comment: DRAGEN gVCF files and joint calling GATK-GenomicsDB
16 months ago by
DBScan
▴ 530
0
votes
0
replies
2.4k
views
Comment:
Comment: Why are the basics so complicated? Basic coverage filtering for VCF files
17 months ago by
DBScan
▴ 530
0
votes
0
replies
2.2k
views
Comment:
Comment: t-test in two groups, multiple rows
18 months ago by
DBScan
▴ 530
0
votes
0
replies
2.2k
views
Answer:
Answer: gnomAD4.0 Hail Table Downloading
18 months ago by
DBScan
▴ 530
1
vote
0
replies
1.4k
views
Comment:
Comment: HLA genotyping of whole genome sequencing data
19 months ago by
DBScan
▴ 530
3
votes
1
reply
4.8k
views
Answer:
Answer: Nextflow and self-made pipelines opinion
19 months ago by
DBScan
▴ 530
1
vote
0
replies
1.3k
views
Comment:
Comment: CNV benchmarking: Truvari & HG002 SVs v0.6 (GIAB)
19 months ago by
DBScan
▴ 530
0
votes
1
reply
1.3k
views
Comment:
Comment: CNV benchmarking: Truvari & HG002 SVs v0.6 (GIAB)
19 months ago by
DBScan
▴ 530
0
votes
1
reply
3.5k
views
Comment:
Comment: jellyfish installed in conda, but 'command not found' when I try to run it
19 months ago by
DBScan
▴ 530
0
votes
1
reply
3.5k
views
Comment:
Comment: jellyfish installed in conda, but 'command not found' when I try to run it
19 months ago by
DBScan
▴ 530
0
votes
1
reply
1.4k
views
Answer:
Answer: how to extract variants from the vcf.gz files linked below?
19 months ago by
DBScan
▴ 530
0
votes
1
reply
671
views
Comment:
Comment: Snakemake Wildcard Issue: Trouble Passing Config Field to Rule Input
19 months ago by
DBScan
▴ 530
0
votes
0
replies
1.5k
views
Comment:
Comment: PCA from plink2 for SGDP using a pangenome and DeepVariant
19 months ago by
DBScan
▴ 530
0
votes
1
reply
1.5k
views
Comment:
Comment: PCA from plink2 for SGDP using a pangenome and DeepVariant
19 months ago by
DBScan
▴ 530
0
votes
1
reply
1.5k
views
Comment:
Comment: PCA from plink2 for SGDP using a pangenome and DeepVariant
19 months ago by
DBScan
▴ 530
0
votes
0
replies
2.4k
views
Comment:
Comment: difference betwween hail and plink
19 months ago by
DBScan
▴ 530
1
vote
1
reply
1.2k
views
Answer:
Answer: What is the best GWAS tool to use for a very large cohort data (UK Biobank data)
19 months ago by
DBScan
▴ 530
0
votes
1
reply
2.0k
views
Comment:
Comment: PCA plot interpretation (single population)
19 months ago by
DBScan
▴ 530
0
votes
1
reply
1.8k
views
Answer:
Answer: fill-from-fasta doesnt fill missing values in REF
20 months ago by
DBScan
▴ 530
0
votes
0
replies
1.5k
views
Comment:
Comment: Normal number of variants to lose during liftover: GRCh38 to hg19
20 months ago by
DBScan
▴ 530
1
vote
1
reply
1.3k
views
Answer:
Answer: Suggestions for a simpler solution for collecting snakemake rule output in a tex
20 months ago by
DBScan
▴ 530
0
votes
0
replies
2.2k
views
Comment:
Comment: Problem with DRAGEN RNAseq hashtable directory
20 months ago by
DBScan
▴ 530
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