Profile Posts Awards
Show
all questions tools blogs news tutorials forum answers comments
Showing : comments
1
vote
1
reply
761
views
Comment: Comment: Filtering Multi-sample VCF file for all except one Genotype
11 days ago by Jeremy Leipzig 22k
0
votes
0
replies
761
views
Comment: Comment: Filtering Multi-sample VCF file for all except one Genotype
13 days ago by Jeremy Leipzig 22k
2
votes
0
replies
2.3k
views
Comment: Comment: NGS forensics: how to know if data is fabricated
22 days ago by Jeremy Leipzig 22k
0
votes
1
reply
620
views
Comment: Comment: gvcf joint calling
22 days ago by Jeremy Leipzig 22k
0
votes
1
reply
620
views
Comment: Comment: gvcf joint calling
23 days ago by Jeremy Leipzig 22k
1
vote
0
replies
309
views
Comment: Comment: CombineGVCFs vs. MergeVcfs
4 weeks ago by Jeremy Leipzig 22k
0
votes
1
reply
748
views
Comment: Comment: Why are the basics so complicated? Basic coverage filtering for VCF files
5 weeks ago by Jeremy Leipzig 22k
0
votes
0
replies
336
views
Comment: Comment: Bioinformatics variant calling software
6 weeks ago by Jeremy Leipzig 22k
0
votes
0
replies
250
views
Comment: Comment: AUC=1, is it possible after lasso regression?
7 weeks ago by Jeremy Leipzig 22k
0
votes
1
reply
470
views
Comment: Comment: I can't add VAF from population for all of my variants from VCF file
10 weeks ago by Jeremy Leipzig 22k
1
vote
1
reply
531
views
Comment: Comment: Snakemake rule that runs an assessment for once after completing other previous
10 weeks ago by Jeremy Leipzig 22k
1
vote
1
reply
531
views
Comment: Comment: Snakemake rule that runs an assessment for once after completing other previous
10 weeks ago by Jeremy Leipzig 22k
1
vote
0
replies
1.5k
views
Comment: Comment: Novel sparse optimisation for high accuracy cancer classification on the 33-canc
10 weeks ago by Jeremy Leipzig 22k
0
votes
2
replies
531
views
Comment: Comment: Snakemake rule that runs an assessment for once after completing other previous
10 weeks ago by Jeremy Leipzig 22k
1
vote
1
reply
502
views
Comment: Comment: Snakemake: how to define output from a dictionary according to wildcard
11 weeks ago by Jeremy Leipzig 22k
0
votes
0
replies
268
views
Comment: Comment: Resolution of ambiguous calls in germline vcf
11 weeks ago by Jeremy Leipzig 22k
0
votes
1
reply
847
views
Comment: Comment: What is the expected number of common/mutual/shared SNVs between two, three, fou
12 weeks ago by Jeremy Leipzig 22k
0
votes
1
reply
847
views
Comment: Comment: What is the expected number of common/mutual/shared SNVs between two, three, fou
12 weeks ago by Jeremy Leipzig 22k
1
vote
1
reply
31k
views
Comment: Comment: List of cloud genomics companies
3 months ago by Jeremy Leipzig 22k
1
vote
0
replies
24k
views
Comment: Comment: Difference between tSNE and PCA analysis
3 months ago by Jeremy Leipzig 22k
0
votes
1
reply
489
views
Comment: Comment: how to extract variants from the vcf.gz files linked below?
3 months ago by Jeremy Leipzig 22k
0
votes
0
replies
31k
views
Comment: Comment: List of cloud genomics companies
3 months ago by Jeremy Leipzig 22k
1
vote
0
replies
31k
views
Comment: Comment: List of cloud genomics companies
3 months ago by Jeremy Leipzig 22k
1
vote
1
reply
415
views
Comment: Comment: Linear Mixed-Effects Model Coefficient Interpretation
3 months ago by Jeremy Leipzig 22k
1
vote
1
reply
734
views
Comment: Comment: difference betwween hail and plink
3 months ago by Jeremy Leipzig 22k
0
votes
0
replies
447
views
Comment: Comment: How to reference input variable in output section of rule of Snakemake rule
3 months ago by Jeremy Leipzig 22k
0
votes
1
reply
493
views
Comment: Comment: 1000 Genome: Cause of duplicate variants with different genotypes
3 months ago by Jeremy Leipzig 22k
0
votes
1
reply
493
views
Comment: Comment: 1000 Genome: Cause of duplicate variants with different genotypes
3 months ago by Jeremy Leipzig 22k
0
votes
0
replies
592
views
Comment: Comment: What tools exist for filtering hundreds of VCFs (and annotated into VCFs in txt
3 months ago by Jeremy Leipzig 22k
0
votes
0
replies
449
views
Comment: Comment: How quickly can an SRA submission proceed directly from S3
3 months ago by Jeremy Leipzig 22k
0
votes
1
reply
449
views
Comment: Comment: How quickly can an SRA submission proceed directly from S3
3 months ago by Jeremy Leipzig 22k
0
votes
0
replies
857
views
Comment: Comment: Isolating and extracting regions in VCF file
3 months ago by Jeremy Leipzig 22k
0
votes
1
reply
766
views
Comment: Comment: GIAB Benchmarking
4 months ago by Jeremy Leipzig 22k
0
votes
0
replies
495
views
Comment: Comment: Tool to Create Sequence Logo Plot with Indels or Alignment-Aware Position Freque
4 months ago by Jeremy Leipzig 22k
2
votes
2
replies
1.3k
views
Comment: Comment: Problem with Mamba
5 months ago by Jeremy Leipzig 22k
0
votes
0
replies
749
views
Comment: Comment: Multiallelic variants when merging VCF's with GLnexus
5 months ago by Jeremy Leipzig 22k
0
votes
1
reply
749
views
Comment: Comment: Multiallelic variants when merging VCF's with GLnexus
5 months ago by Jeremy Leipzig 22k
0
votes
0
replies
1.8k
views
Comment: Comment: How to query 1000 genomes project VCF files for specific regions without downloa
5 months ago by Jeremy Leipzig 22k
0
votes
1
reply
749
views
Comment: Comment: Multiallelic variants when merging VCF's with GLnexus
5 months ago by Jeremy Leipzig 22k
3
votes
0
replies
967
views
Comment: Comment: Individual vs. joint call VCFs
5 months ago by Jeremy Leipzig 22k
0
votes
1
reply
967
views
Comment: Comment: Individual vs. joint call VCFs
5 months ago by Jeremy Leipzig 22k
0
votes
0
replies
2.7k
views
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
0
votes
0
replies
324
views
Comment: Comment: Bgen file not being opened by PRSice
6 months ago by Jeremy Leipzig 22k
1
vote
1
reply
971
views
Comment: Comment: How to create a Venn Diagram for overlapping SVs from a merged VCF
6 months ago by Jeremy Leipzig 22k
0
votes
0
replies
926
views
Comment: Comment: Isaac aligner V4 genome aligner questions
6 months ago by Jeremy Leipzig 22k
1
vote
0
replies
507
views
Comment: Comment: How to find the Allele Number (AN) of a variant not reported on gnomAD
6 months ago by Jeremy Leipzig 22k
1
vote
1
reply
971
views
Comment: Comment: How to create a Venn Diagram for overlapping SVs from a merged VCF
6 months ago by Jeremy Leipzig 22k
1
vote
1
reply
971
views
Comment: Comment: How to create a Venn Diagram for overlapping SVs from a merged VCF
6 months ago by Jeremy Leipzig 22k
0
votes
1
reply
753
views
Comment: Comment: Calculating ROC50 in R
6 months ago by Jeremy Leipzig 22k
0
votes
1
reply
753
views
Comment: Comment: Calculating ROC50 in R
6 months ago by Jeremy Leipzig 22k
816 results • Page 1 of 17
Content Search
Users
Tags
Badges
Help About
FAQ
Access RSS
API
Stats

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.

Powered by the version 2.3.6