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Comment:
Comment: Why are the basics so complicated? Basic coverage filtering for VCF files
19 days ago by
DBScan
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798
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Comment:
Comment: t-test in two groups, multiple rows
6 weeks ago by
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791
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Answer:
Answer: gnomAD4.0 Hail Table Downloading
6 weeks ago by
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393
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Comment:
Comment: HLA genotyping of whole genome sequencing data
8 weeks ago by
DBScan
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985
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Answer:
Answer: Nextflow and self-made pipelines opinion
8 weeks ago by
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347
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Comment:
Comment: CNV benchmarking: Truvari & HG002 SVs v0.6 (GIAB)
8 weeks ago by
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347
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Comment:
Comment: CNV benchmarking: Truvari & HG002 SVs v0.6 (GIAB)
8 weeks ago by
DBScan
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814
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Comment:
Comment: jellyfish installed in conda, but 'command not found' when I try to run it
9 weeks ago by
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814
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Comment:
Comment: jellyfish installed in conda, but 'command not found' when I try to run it
9 weeks ago by
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433
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Answer:
Answer: how to extract variants from the vcf.gz files linked below?
9 weeks ago by
DBScan
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260
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Comment:
Comment: Snakemake Wildcard Issue: Trouble Passing Config Field to Rule Input
10 weeks ago by
DBScan
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468
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Comment:
Comment: PCA from plink2 for SGDP using a pangenome and DeepVariant
10 weeks ago by
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468
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Comment:
Comment: PCA from plink2 for SGDP using a pangenome and DeepVariant
11 weeks ago by
DBScan
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468
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Comment:
Comment: PCA from plink2 for SGDP using a pangenome and DeepVariant
11 weeks ago by
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652
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Comment:
Comment: difference betwween hail and plink
11 weeks ago by
DBScan
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1
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1
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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
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588
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Comment:
Comment: PCA plot interpretation (single population)
12 weeks ago by
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587
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Answer:
Answer: fill-from-fasta doesnt fill missing values in REF
3 months ago by
DBScan
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496
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Comment:
Comment: Normal number of variants to lose during liftover: GRCh38 to hg19
3 months ago by
DBScan
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1
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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
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702
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Comment:
Comment: Problem with DRAGEN RNAseq hashtable directory
3 months ago by
DBScan
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0
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2
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702
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Answer:
Answer: Problem with DRAGEN RNAseq hashtable directory
3 months ago by
DBScan
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350
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Answer:
Answer: how to merge two files without duplicating same column
3 months ago by
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702
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Comment:
Comment: GIAB Benchmarking
3 months ago by
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628
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Comment:
Comment: Calculating number of SNPs in linkage disequilibrium at different thresholds fro
3 months ago by
DBScan
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414
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Comment:
Comment: GATK version check failed
3 months ago by
DBScan
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1
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0
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893
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Comment:
Comment: Problem in installing 'magick' R package
5 months ago by
DBScan
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2
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1
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857
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Answer:
Answer: Snakemake alignment script
7 months ago by
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593
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Comment:
Comment: Saving the output of LD pruning from SNPRelate package as a new GDS file
7 months ago by
DBScan
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505
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Answer:
Answer: VCF QUAL field for multiple samples
7 months ago by
DBScan
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2
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1.2k
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Comment:
Comment: T2T fixed GRCg38 gaps and issues, gaps genomic coordinates.
8 months ago by
DBScan
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1.2k
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Comment:
Comment: T2T fixed GRCg38 gaps and issues, gaps genomic coordinates.
8 months ago by
DBScan
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0
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1
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698
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Answer:
Answer: BWA-mem2 vs Bowtie2: no deterministic option
8 months ago by
DBScan
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3
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1
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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
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753
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Answer:
Answer: vcf file
8 months ago by
DBScan
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0
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0
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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
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1
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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
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0
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1
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748
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Comment:
Comment: bcftools view to failed reader data
9 months ago by
DBScan
▴ 300
2
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1
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748
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Answer:
Answer: bcftools view to failed reader data
9 months ago by
DBScan
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1
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1
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3.0k
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Comment:
Comment: Conda/Mamba environment activation error
9 months ago by
DBScan
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2
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1
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3.0k
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Answer:
Answer: Conda/Mamba environment activation error
9 months ago by
DBScan
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0
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0
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1.1k
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Answer:
Answer: Rstudio server in Snakemake
9 months ago by
DBScan
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1
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0
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1.1k
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Comment:
Comment: Qualimap multi-bamqc input file
9 months ago by
DBScan
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1
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1.1k
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Comment:
Comment: Qualimap multi-bamqc input file
9 months ago by
DBScan
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0
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1
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695
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Comment:
Comment: whole genome sequencing and assembly
9 months ago by
DBScan
▴ 300
0
votes
1
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695
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Comment:
Comment: whole genome sequencing and assembly
9 months ago by
DBScan
▴ 300
0
votes
1
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709
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Comment:
Comment: Deepvariant and input CRAM files
9 months ago by
DBScan
▴ 300
0
votes
0
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497
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Answer:
Answer: BWA MEM -K option
9 months ago by
DBScan
▴ 300
0
votes
1
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689
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Answer:
Answer: strelka variant calling
9 months ago by
DBScan
▴ 300
0
votes
1
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774
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Comment:
Comment: Launched: Genozip 15 with co-compression of BAM and FASTQ
10 months ago by
DBScan
▴ 300
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