Profile Posts Awards
Show
all questions tools blogs news tutorials forum answers comments
5
votes
5
replies
4.3k
views
Error: htsjdk.tribble.TribbleExpection: The provided VCF file is malformed at approximately line number 5880: Duplicate allele added to VariantContex…
SNP genome next-gen Assembly
updated 22 months ago by ▴ 70 • written 4.4 years ago by ▴ 540
0
votes
2
replies
3.9k
views
Sleuth_fit error "`Error in if (sum(valid) == 0) { : missing value where TRUE/FALSE needed"
R rna-seq software error Assembly
updated 3.4 years ago by ▴ 370 • written 7.6 years ago by ▴ 540
3
votes
1
reply
1.2k
views
Liftover using gVCF
genome assembly GATK liftover
updated 3.5 years ago by ★ 4.8k • written 3.5 years ago by ▴ 540
0
votes
1
reply
1.2k
views
Running SnpSift in parallel
VCF WGS Annotation
updated 3.7 years ago by 166k • written 3.7 years ago by ▴ 540
0
votes
0
replies
1.6k
views
Comment: Comment: Case Control count per variant
3.8 years ago by williamsbrian5064 ▴ 540
0
votes
1
reply
1.6k
views
Comment: Comment: Case Control count per variant
3.8 years ago by williamsbrian5064 ▴ 540
1
vote
4
replies
1.6k
views
Case Control count per variant
WGS VCF Annotation NGS
3.8 years ago by williamsbrian5064 ▴ 540
0
votes
1
reply
3.3k
views
Comment: Comment: Get REVEL plugin started with VEP
3.9 years ago by williamsbrian5064 ▴ 540
0
votes
3
replies
1.5k
views
Comment: Comment: How to calculate combined expression of two genes
4.1 years ago by williamsbrian5064 ▴ 540
4
votes
5
replies
1.5k
views
How to calculate combined expression of two genes
R rna-seq
updated 4.1 years ago by 89k • written 4.1 years ago by ▴ 540
4
votes
4
replies
3.2k
views
GATK markduplicates out of memory
Assembly WGS MarkDuplicates GATK
updated 4.1 years ago by 166k • written 4.1 years ago by ▴ 540
0
votes
1
reply
3.2k
views
Comment: Comment: GATK markduplicates out of memory
4.1 years ago by williamsbrian5064 ▴ 540
6
votes
2
replies
2.5k
views
bcftools vcf2sex
genomics genome alignment genotyping
updated 4.2 years ago by ★ 1.5k • written 4.2 years ago by ▴ 540
0
votes
1
reply
4.1k
views
Comment: C: PLINK:Error: Variant '.' is not biallelic. To obtain a full list of merge failur
4.3 years ago by williamsbrian5064 ▴ 540
0
votes
0
replies
4.1k
views
Comment: C: PLINK:Error: Variant '.' is not biallelic. To obtain a full list of merge failur
4.3 years ago by williamsbrian5064 ▴ 540
3
votes
5
replies
4.1k
views
PLINK:Error: Variant '.' is not biallelic. To obtain a full list of merge failures
SNP Assembly genome next-gen
4.3 years ago by williamsbrian5064 ▴ 540
0
votes
1
reply
4.3k
views
Comment: C: bcftools +fill-tag does not work in loop
4.3 years ago by williamsbrian5064 ▴ 540
0
votes
0
replies
2.9k
views
Comment: C: Minor allele count report with --freq count in PLINK2
4.3 years ago by williamsbrian5064 ▴ 540
0
votes
1
reply
4.3k
views
Comment: C: bcftools +fill-tag does not work in loop
4.3 years ago by williamsbrian5064 ▴ 540
0
votes
0
replies
2.7k
views
Comment: C: Remove Chr:position format to just Chr
4.3 years ago by williamsbrian5064 ▴ 540
1
vote
1
reply
2.7k
views
Comment: C: Remove Chr:position format to just Chr
4.3 years ago by williamsbrian5064 ▴ 540
0
votes
0
replies
2.7k
views
Comment: C: Remove Chr:position format to just Chr
4.3 years ago by williamsbrian5064 ▴ 540
0
votes
1
reply
2.9k
views
Comment: C: Minor allele count report with --freq count in PLINK2
4.3 years ago by williamsbrian5064 ▴ 540
1
vote
2
replies
2.7k
views
Answer: A: Remove Chr:position format to just Chr
4.3 years ago by williamsbrian5064 ▴ 540
0
votes
0
replies
2.7k
views
Comment: C: Remove Chr:position format to just Chr
4.3 years ago by williamsbrian5064 ▴ 540
0
votes
1
reply
1.5k
views
Answer: A: Get TSS information from GFF3 file depending on strand
4.3 years ago by williamsbrian5064 ▴ 540
2
votes
0
replies
782
views
Comment: C: Different symbols in genotype field in VCF files
4.3 years ago by williamsbrian5064 ▴ 540
0
votes
0
replies
6.0k
views
Comment: C: Remove uncharacterized chromosomes from reference fasta file
4.3 years ago by williamsbrian5064 ▴ 540
0
votes
0
replies
6.0k
views
Comment: C: Remove uncharacterized chromosomes from reference fasta file
4.3 years ago by williamsbrian5064 ▴ 540
3
votes
1
reply
6.0k
views
Comment: C: Remove uncharacterized chromosomes from reference fasta file
4.3 years ago by williamsbrian5064 ▴ 540
17
votes
7
replies
6.0k
views
Remove uncharacterized chromosomes from reference fasta file
Assembly genome sequence next-gen
updated 4.3 years ago by 13k • written 4.3 years ago by ▴ 540
0
votes
0
replies
4.7k
views
Comment: C: How to sort fasta file numerically
4.3 years ago by williamsbrian5064 ▴ 540
0
votes
0
replies
4.7k
views
Comment: C: How to sort fasta file numerically
4.3 years ago by williamsbrian5064 ▴ 540
0
votes
1
reply
4.7k
views
Comment: C: How to sort fasta file numerically
4.3 years ago by williamsbrian5064 ▴ 540
0
votes
1
reply
4.7k
views
Comment: C: How to sort fasta file numerically
4.3 years ago by williamsbrian5064 ▴ 540
11
votes
8
replies
4.7k
views
How to sort fasta file numerically
Assembly genome sequence
updated 4.3 years ago by 88k • written 4.3 years ago by ▴ 540
4
votes
3
replies
8.6k
views
Samtools bam2fq converting bam file to fastq. What happens to unmapped reads?
Assembly alignment sequencing next-gen
updated 4.4 years ago by 15k • written 4.4 years ago by ▴ 540
0
votes
0
replies
1.5k
views
Comment: C: Error occur during tophat2 downloading
4.4 years ago by williamsbrian5064 ▴ 540
0
votes
1
reply
4.3k
views
Comment: C: Error: htsjdk.tribble.TribbleExpection: The provided VCF file is malformed at ap
4.4 years ago by williamsbrian5064 ▴ 540
0
votes
1
reply
1.3k
views
Computing all possible single amino acid substitutions for a protein
genome gene
updated 4.5 years ago by • 0 • written 6.0 years ago by ▴ 540
0
votes
1
reply
2.7k
views
Comment: C: How to remove contamination from WGS fastq files
4.7 years ago by williamsbrian5064 ▴ 540
0
votes
1
reply
2.7k
views
Comment: C: How to remove contamination from WGS fastq files
4.7 years ago by williamsbrian5064 ▴ 540
0
votes
1
reply
2.7k
views
Comment: C: How to remove contamination from WGS fastq files
4.7 years ago by williamsbrian5064 ▴ 540
8
votes
10
replies
2.7k
views
How to remove contamination from WGS fastq files
next-gen sequence
updated 4.7 years ago by 151k • written 4.7 years ago by ▴ 540
0
votes
1
reply
2.7k
views
Comment: C: How to remove contamination from WGS fastq files
4.7 years ago by williamsbrian5064 ▴ 540
1
vote
0
replies
6.5k
views
Comment: C: No alias or index file found for protein database
5.7 years ago by williamsbrian5064 ▴ 540
0
votes
0
replies
6.5k
views
Comment: C: No alias or index file found for protein database
5.7 years ago by williamsbrian5064 ▴ 540
0
votes
1
reply
22k
views
Comment: C: Best tool for variant calling
5.7 years ago by williamsbrian5064 ▴ 540
0
votes
2
replies
979
views
samtools having to use -A input option
assembly next-gen genome alignment
5.9 years ago by williamsbrian5064 ▴ 540
17
votes
37
replies
6.5k
views
No alias or index file found for protein database
next-gen software error sequence
updated 6.1 years ago by 20 • written 6.2 years ago by ▴ 540
195 results • Page 1 of 4
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