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Comment: Comment: Filtering Multi-sample VCF file for all except one Genotype
11 days ago by Jeremy Leipzig 22k
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755
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Comment: Comment: Filtering Multi-sample VCF file for all except one Genotype
13 days ago by Jeremy Leipzig 22k
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2.3k
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Comment: Comment: NGS forensics: how to know if data is fabricated
22 days ago by Jeremy Leipzig 22k
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1
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620
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Comment: Comment: gvcf joint calling
22 days ago by Jeremy Leipzig 22k
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620
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Comment: Comment: gvcf joint calling
23 days ago by Jeremy Leipzig 22k
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0
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307
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Comment: Comment: CombineGVCFs vs. MergeVcfs
4 weeks ago by Jeremy Leipzig 22k
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1
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743
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Comment: Comment: Why are the basics so complicated? Basic coverage filtering for VCF files
5 weeks ago by Jeremy Leipzig 22k
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334
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Comment: Comment: Bioinformatics variant calling software
6 weeks ago by Jeremy Leipzig 22k
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249
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Comment: Comment: AUC=1, is it possible after lasso regression?
6 weeks ago by Jeremy Leipzig 22k
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470
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Comment: Comment: I can't add VAF from population for all of my variants from VCF file
10 weeks ago by Jeremy Leipzig 22k
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527
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Comment: Comment: Snakemake rule that runs an assessment for once after completing other previous
10 weeks ago by Jeremy Leipzig 22k
1
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1
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527
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Comment: Comment: Snakemake rule that runs an assessment for once after completing other previous
10 weeks ago by Jeremy Leipzig 22k
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1.5k
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Comment: Comment: Novel sparse optimisation for high accuracy cancer classification on the 33-canc
10 weeks ago by Jeremy Leipzig 22k
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2
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527
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Comment: Comment: Snakemake rule that runs an assessment for once after completing other previous
10 weeks ago by Jeremy Leipzig 22k
1
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1
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500
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Comment: Comment: Snakemake: how to define output from a dictionary according to wildcard
11 weeks ago by Jeremy Leipzig 22k
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268
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Comment: Comment: Resolution of ambiguous calls in germline vcf
11 weeks ago by Jeremy Leipzig 22k
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845
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Comment: Comment: What is the expected number of common/mutual/shared SNVs between two, three, fou
12 weeks ago by Jeremy Leipzig 22k
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1
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845
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Comment: Comment: What is the expected number of common/mutual/shared SNVs between two, three, fou
12 weeks ago by Jeremy Leipzig 22k
1
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1
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31k
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Comment: Comment: List of cloud genomics companies
12 weeks ago by Jeremy Leipzig 22k
1
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0
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24k
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Comment: Comment: Difference between tSNE and PCA analysis
3 months ago by Jeremy Leipzig 22k
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486
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Comment: Comment: how to extract variants from the vcf.gz files linked below?
3 months ago by Jeremy Leipzig 22k
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31k
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Comment: Comment: List of cloud genomics companies
3 months ago by Jeremy Leipzig 22k
1
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0
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31k
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Comment: Comment: List of cloud genomics companies
3 months ago by Jeremy Leipzig 22k
1
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1
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414
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Comment: Comment: Linear Mixed-Effects Model Coefficient Interpretation
3 months ago by Jeremy Leipzig 22k
1
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730
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Comment: Comment: difference betwween hail and plink
3 months ago by Jeremy Leipzig 22k
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445
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Comment: Comment: How to reference input variable in output section of rule of Snakemake rule
3 months ago by Jeremy Leipzig 22k
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1
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490
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Comment: Comment: 1000 Genome: Cause of duplicate variants with different genotypes
3 months ago by Jeremy Leipzig 22k
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1
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490
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Comment: Comment: 1000 Genome: Cause of duplicate variants with different genotypes
3 months ago by Jeremy Leipzig 22k
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590
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Comment: Comment: What tools exist for filtering hundreds of VCFs (and annotated into VCFs in txt
3 months ago by Jeremy Leipzig 22k
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444
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Comment: Comment: How quickly can an SRA submission proceed directly from S3
3 months ago by Jeremy Leipzig 22k
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1
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444
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Comment: Comment: How quickly can an SRA submission proceed directly from S3
3 months ago by Jeremy Leipzig 22k
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0
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854
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Comment: Comment: Isolating and extracting regions in VCF file
3 months ago by Jeremy Leipzig 22k
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1
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765
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Comment: Comment: GIAB Benchmarking
4 months ago by Jeremy Leipzig 22k
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0
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494
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Comment: Comment: Tool to Create Sequence Logo Plot with Indels or Alignment-Aware Position Freque
4 months ago by Jeremy Leipzig 22k
2
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2
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1.3k
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Comment: Comment: Problem with Mamba
5 months ago by Jeremy Leipzig 22k
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745
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Comment: Comment: Multiallelic variants when merging VCF's with GLnexus
5 months ago by Jeremy Leipzig 22k
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1
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745
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Comment: Comment: Multiallelic variants when merging VCF's with GLnexus
5 months ago by Jeremy Leipzig 22k
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0
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1.8k
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Comment: Comment: How to query 1000 genomes project VCF files for specific regions without downloa
5 months ago by Jeremy Leipzig 22k
0
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1
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745
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Comment: Comment: Multiallelic variants when merging VCF's with GLnexus
5 months ago by Jeremy Leipzig 22k
3
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966
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Comment: Comment: Individual vs. joint call VCFs
5 months ago by Jeremy Leipzig 22k
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1
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966
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Comment: Comment: Individual vs. joint call VCFs
5 months ago by Jeremy Leipzig 22k
0
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0
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2.7k
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Comment: Comment: How to display a VCF/BCF file or stream as a paginated table in a python web fra
5 months ago by Jeremy Leipzig 22k
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0
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324
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Comment: Comment: Bgen file not being opened by PRSice
6 months ago by Jeremy Leipzig 22k
1
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1
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969
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Comment: Comment: How to create a Venn Diagram for overlapping SVs from a merged VCF
6 months ago by Jeremy Leipzig 22k
0
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0
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926
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Comment: Comment: Isaac aligner V4 genome aligner questions
6 months ago by Jeremy Leipzig 22k
1
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0
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507
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Comment: Comment: How to find the Allele Number (AN) of a variant not reported on gnomAD
6 months ago by Jeremy Leipzig 22k
1
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1
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969
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Comment: Comment: How to create a Venn Diagram for overlapping SVs from a merged VCF
6 months ago by Jeremy Leipzig 22k
1
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1
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969
views
Comment: Comment: How to create a Venn Diagram for overlapping SVs from a merged VCF
6 months ago by Jeremy Leipzig 22k
0
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1
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752
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Comment: Comment: Calculating ROC50 in R
6 months ago by Jeremy Leipzig 22k
0
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1
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752
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Comment: Comment: Calculating ROC50 in R
6 months ago by Jeremy Leipzig 22k
816 results • Page 1 of 17
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