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Comment: Comment: Use of gVCF by clinical sequencing labs
11 months ago by Jeremy Leipzig 23k
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771
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Answer: Answer: Where can I find a database of healthy genotypes as well as a database of geneti
11 months ago by Jeremy Leipzig 23k
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Answer: Answer: Can't reproduce harmony results in Seurat
12 months ago by Jeremy Leipzig 23k
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722
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Answer: Answer: Why does the AD value of my VCF file display 3 values?
12 months ago by Jeremy Leipzig 23k
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1.4k
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Comment: Comment: Ancestry estimation using 1000 genomes as reference
12 months ago by Jeremy Leipzig 23k
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912
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Answer: Answer: How can we determine or find the insertion time of Numts?
13 months ago by Jeremy Leipzig 23k
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2.9k
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Comment: Comment: Proper reanotation of genepanel with snpEff and dbNSFP
13 months ago by Jeremy Leipzig 23k
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2.9k
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Comment: Comment: Proper reanotation of genepanel with snpEff and dbNSFP
13 months ago by Jeremy Leipzig 23k
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2.9k
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Comment: Comment: Proper reanotation of genepanel with snpEff and dbNSFP
13 months ago by Jeremy Leipzig 23k
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2.9k
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Comment: Comment: Proper reanotation of genepanel with snpEff and dbNSFP
13 months ago by Jeremy Leipzig 23k
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2.9k
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Answer: Answer: Proper reanotation of genepanel with snpEff and dbNSFP
13 months ago by Jeremy Leipzig 23k
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2.4k
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Answer: Answer: looking for 1000g hg38 reference data to anchor with my genomic data to plot th
14 months ago by Jeremy Leipzig 23k
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960
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Answer: Answer: GATK GenomicsDBImport update database error using snakemake
14 months ago by Jeremy Leipzig 23k
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1.4k
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Answer: Answer: How can I get an allele count table from a .vcf file?
14 months ago by Jeremy Leipzig 23k
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728
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Comment: Comment: Count and filter sites with degenarate bases in VCF files
14 months ago by Jeremy Leipzig 23k
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1.6k
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Comment: Comment: Does PRS distribution of target data should follow gaussian distribution?
15 months ago by Jeremy Leipzig 23k
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987
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Answer: Answer: VCFtools indels/SNP treatment
15 months ago by Jeremy Leipzig 23k
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987
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Comment: Comment: VCFtools indels/SNP treatment
15 months ago by Jeremy Leipzig 23k
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2.6k
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Answer: Answer: Alignment tool for very short reads (25bp)
15 months ago by Jeremy Leipzig 23k
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1.6k
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Comment: Comment: Looking for clarification of .vcf output from variant calling
15 months ago by Jeremy Leipzig 23k
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1.6k
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Comment: Comment: Looking for clarification of .vcf output from variant calling
15 months ago by Jeremy Leipzig 23k
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1
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1.6k
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Answer: Answer: Looking for clarification of .vcf output from variant calling
15 months ago by Jeremy Leipzig 23k
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1.3k
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Comment: Comment: Could not parse a VCF file when using bcftools annotate
15 months ago by Jeremy Leipzig 23k
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859
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Comment: Comment: Intersection of multiple vcf files
15 months ago by Jeremy Leipzig 23k
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4.2k
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Comment: Comment: Venter Genome Vcf
15 months ago by Jeremy Leipzig 23k
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1.3k
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Answer: Answer: Why some SNP's allele frequencies in gnomAD are so different between v2 and v4?
15 months ago by Jeremy Leipzig 23k
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1.2k
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Answer: Answer: Would you bother re-mapping RNA-seq data from an old GRCh38 build to a newer ver
16 months ago by Jeremy Leipzig 23k
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2.0k
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Comment: Comment: Filtering Multi-sample VCF file for all except one Genotype
16 months ago by Jeremy Leipzig 23k
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2.0k
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Comment: Comment: Filtering Multi-sample VCF file for all except one Genotype
16 months ago by Jeremy Leipzig 23k
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6.0k
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Comment: Comment: NGS forensics: how to know if data is fabricated
16 months ago by Jeremy Leipzig 23k
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2.0k
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Comment: Comment: gvcf joint calling
16 months ago by Jeremy Leipzig 23k
4
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1
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6.0k
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Answer: Answer: NGS forensics: how to know if data is fabricated
16 months ago by Jeremy Leipzig 23k
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2.0k
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Comment: Comment: gvcf joint calling
16 months ago by Jeremy Leipzig 23k
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1
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2.0k
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Answer: Answer: gvcf joint calling
16 months ago by Jeremy Leipzig 23k
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1.6k
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Comment: Comment: CombineGVCFs vs. MergeVcfs
17 months ago by Jeremy Leipzig 23k
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2.4k
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Comment: Comment: Why are the basics so complicated? Basic coverage filtering for VCF files
17 months ago by Jeremy Leipzig 23k
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904
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Comment: Comment: Bioinformatics variant calling software
17 months ago by Jeremy Leipzig 23k
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652
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Comment: Comment: AUC=1, is it possible after lasso regression?
17 months ago by Jeremy Leipzig 23k
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1.0k
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Comment: Comment: I can't add VAF from population for all of my variants from VCF file
18 months ago by Jeremy Leipzig 23k
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1.5k
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Comment: Comment: Snakemake rule that runs an assessment for once after completing other previous
18 months ago by Jeremy Leipzig 23k
1
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1
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1.5k
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Comment: Comment: Snakemake rule that runs an assessment for once after completing other previous
18 months ago by Jeremy Leipzig 23k
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0
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3.1k
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Comment: Comment: Novel sparse optimisation for high accuracy cancer classification on the 33-canc
18 months ago by Jeremy Leipzig 23k
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2
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1.5k
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Comment: Comment: Snakemake rule that runs an assessment for once after completing other previous
18 months ago by Jeremy Leipzig 23k
1
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1
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1.9k
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Comment: Comment: Snakemake: how to define output from a dictionary according to wildcard
18 months ago by Jeremy Leipzig 23k
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0
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793
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Comment: Comment: Resolution of ambiguous calls in germline vcf
18 months ago by Jeremy Leipzig 23k
3
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4.8k
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Answer: Answer: Nextflow and self-made pipelines opinion
18 months ago by Jeremy Leipzig 23k
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1
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1.9k
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Comment: Comment: What is the expected number of common/mutual/shared SNVs between two, three, fou
18 months ago by Jeremy Leipzig 23k
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1.9k
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Comment: Comment: What is the expected number of common/mutual/shared SNVs between two, three, fou
19 months ago by Jeremy Leipzig 23k
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1
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35k
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Comment: Comment: List of cloud genomics companies
19 months ago by Jeremy Leipzig 23k
1
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0
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27k
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Comment: Comment: Difference between tSNE and PCA analysis
19 months ago by Jeremy Leipzig 23k
1,409 results • Page 2 of 29
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