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2.8k
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Comment: Comment: failing to install rMATS
12 months ago by Jeremy Leipzig 23k
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0
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1.2k
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Comment: Comment: Snakemake expand(): using a helper function (zip) and imputing wildcards?
12 months ago by Jeremy Leipzig 23k
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2
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1.3k
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Answer: Answer: Why higher read counts in chromosome M/MT
12 months ago by Jeremy Leipzig 23k
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1.4k
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Comment: Comment: Overlapping reads, how do we counter them while variant calling, haplotype calli
12 months ago by Jeremy Leipzig 23k
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1
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1.4k
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Comment: Comment: Overlapping reads, how do we counter them while variant calling, haplotype calli
12 months ago by Jeremy Leipzig 23k
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1
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1.4k
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Comment: Comment: Overlapping reads, how do we counter them while variant calling, haplotype calli
12 months ago by Jeremy Leipzig 23k
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0
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1.1k
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Answer: Answer: Use of gVCF by clinical sequencing labs
12 months ago by Jeremy Leipzig 23k
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1.1k
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Comment: Comment: Use of gVCF by clinical sequencing labs
12 months ago by Jeremy Leipzig 23k
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854
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Answer: Answer: Where can I find a database of healthy genotypes as well as a database of geneti
13 months ago by Jeremy Leipzig 23k
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2
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3.8k
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Answer: Answer: Can't reproduce harmony results in Seurat
13 months ago by Jeremy Leipzig 23k
2
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801
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Answer: Answer: Why does the AD value of my VCF file display 3 values?
14 months ago by Jeremy Leipzig 23k
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1.6k
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Comment: Comment: Ancestry estimation using 1000 genomes as reference
14 months ago by Jeremy Leipzig 23k
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1
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984
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Answer: Answer: How can we determine or find the insertion time of Numts?
14 months ago by Jeremy Leipzig 23k
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2
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3.2k
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Comment: Comment: Proper reanotation of genepanel with snpEff and dbNSFP
15 months ago by Jeremy Leipzig 23k
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1
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3.2k
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Comment: Comment: Proper reanotation of genepanel with snpEff and dbNSFP
15 months ago by Jeremy Leipzig 23k
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1
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3.2k
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Comment: Comment: Proper reanotation of genepanel with snpEff and dbNSFP
15 months ago by Jeremy Leipzig 23k
2
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1
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3.2k
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Comment: Comment: Proper reanotation of genepanel with snpEff and dbNSFP
15 months ago by Jeremy Leipzig 23k
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3.2k
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Answer: Answer: Proper reanotation of genepanel with snpEff and dbNSFP
15 months ago by Jeremy Leipzig 23k
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0
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2.8k
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Answer: Answer: looking for 1000g hg38 reference data to anchor with my genomic data to plot th
15 months ago by Jeremy Leipzig 23k
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0
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1.1k
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Answer: Answer: GATK GenomicsDBImport update database error using snakemake
15 months ago by Jeremy Leipzig 23k
0
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0
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1.5k
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Answer: Answer: How can I get an allele count table from a .vcf file?
16 months ago by Jeremy Leipzig 23k
0
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0
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803
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Comment: Comment: Count and filter sites with degenarate bases in VCF files
16 months ago by Jeremy Leipzig 23k
1
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1
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1.7k
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Comment: Comment: Does PRS distribution of target data should follow gaussian distribution?
16 months ago by Jeremy Leipzig 23k
2
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0
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1.1k
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Answer: Answer: VCFtools indels/SNP treatment
16 months ago by Jeremy Leipzig 23k
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1
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1.1k
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Comment: Comment: VCFtools indels/SNP treatment
16 months ago by Jeremy Leipzig 23k
1
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1
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3.0k
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Answer: Answer: Alignment tool for very short reads (25bp)
16 months ago by Jeremy Leipzig 23k
1
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0
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1.8k
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Comment: Comment: Looking for clarification of .vcf output from variant calling
16 months ago by Jeremy Leipzig 23k
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1
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1.8k
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Comment: Comment: Looking for clarification of .vcf output from variant calling
16 months ago by Jeremy Leipzig 23k
0
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1
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1.8k
views
Answer: Answer: Looking for clarification of .vcf output from variant calling
16 months ago by Jeremy Leipzig 23k
1
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1
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1.5k
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Comment: Comment: Could not parse a VCF file when using bcftools annotate
17 months ago by Jeremy Leipzig 23k
3
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0
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904
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Comment: Comment: Intersection of multiple vcf files
17 months ago by Jeremy Leipzig 23k
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0
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4.4k
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Comment: Comment: Venter Genome Vcf
17 months ago by Jeremy Leipzig 23k
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0
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1.4k
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Answer: Answer: Why some SNP's allele frequencies in gnomAD are so different between v2 and v4?
17 months ago by Jeremy Leipzig 23k
2
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1.3k
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Answer: Answer: Would you bother re-mapping RNA-seq data from an old GRCh38 build to a newer ver
17 months ago by Jeremy Leipzig 23k
1
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1
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2.2k
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Comment: Comment: Filtering Multi-sample VCF file for all except one Genotype
17 months ago by Jeremy Leipzig 23k
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0
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2.2k
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Comment: Comment: Filtering Multi-sample VCF file for all except one Genotype
18 months ago by Jeremy Leipzig 23k
2
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0
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6.3k
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Comment: Comment: NGS forensics: how to know if data is fabricated
18 months ago by Jeremy Leipzig 23k
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1
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2.1k
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Comment: Comment: gvcf joint calling
18 months ago by Jeremy Leipzig 23k
4
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1
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6.3k
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Answer: Answer: NGS forensics: how to know if data is fabricated
18 months ago by Jeremy Leipzig 23k
0
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1
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2.1k
views
Comment: Comment: gvcf joint calling
18 months ago by Jeremy Leipzig 23k
1
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1
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2.1k
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Answer: Answer: gvcf joint calling
18 months ago by Jeremy Leipzig 23k
1
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0
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1.7k
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Comment: Comment: CombineGVCFs vs. MergeVcfs
18 months ago by Jeremy Leipzig 23k
0
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1
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2.6k
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Comment: Comment: Why are the basics so complicated? Basic coverage filtering for VCF files
18 months ago by Jeremy Leipzig 23k
0
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0
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984
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Comment: Comment: Bioinformatics variant calling software
19 months ago by Jeremy Leipzig 23k
0
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0
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703
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Comment: Comment: AUC=1, is it possible after lasso regression?
19 months ago by Jeremy Leipzig 23k
0
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1
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1.1k
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Comment: Comment: I can't add VAF from population for all of my variants from VCF file
19 months ago by Jeremy Leipzig 23k
1
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1
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1.6k
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Comment: Comment: Snakemake rule that runs an assessment for once after completing other previous
20 months ago by Jeremy Leipzig 23k
1
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1
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1.6k
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Comment: Comment: Snakemake rule that runs an assessment for once after completing other previous
20 months ago by Jeremy Leipzig 23k
1
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0
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3.3k
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Comment: Comment: Novel sparse optimisation for high accuracy cancer classification on the 33-canc
20 months ago by Jeremy Leipzig 23k
0
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2
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1.6k
views
Comment: Comment: Snakemake rule that runs an assessment for once after completing other previous
20 months ago by Jeremy Leipzig 23k
1,416 results • Page 2 of 29
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