Profile Posts Awards
Show
all questions tools blogs news tutorials forum answers comments
1
vote
0
replies
611
views
Comment: Comment: What companies do you recommend for targeted sequencing?
5 months ago by amy__ ▴ 240
4
votes
4
replies
611
views
Forum: What companies do you recommend for targeted sequencing?
Targeted-sequencing
5 months ago by amy__ ▴ 240
0
votes
0
replies
611
views
Comment: Comment: What companies do you recommend for targeted sequencing?
5 months ago by amy__ ▴ 240
0
votes
1
reply
510
views
Comment: Comment: Germline variant - should it be seen in the somatic vcf?
5 months ago by amy__ ▴ 240
0
votes
3
replies
510
views
Germline variant - should it be seen in the somatic vcf?
vcf somatic
updated 5 months ago by 44k • written 5 months ago by ▴ 240
0
votes
0
replies
292
views
Advice on telling if two SNPs are on the same haplotype
ldpair halplotype co-occurance gnomad snp
11 months ago by amy__ ▴ 240
0
votes
0
replies
1.7k
views
Comment: Comment: Help with the new nomenclature of multi-nucleotide variants
11 months ago by amy__ ▴ 240
0
votes
1
reply
1.7k
views
Comment: Comment: Help with the new nomenclature of multi-nucleotide variants
11 months ago by amy__ ▴ 240
0
votes
1
reply
1.7k
views
Comment: Comment: Help with the new nomenclature of multi-nucleotide variants
11 months ago by amy__ ▴ 240
0
votes
1
reply
1.7k
views
Comment: Comment: Help with the new nomenclature of multi-nucleotide variants
11 months ago by amy__ ▴ 240
0
votes
1
reply
1.7k
views
Comment: Comment: Help with the new nomenclature of multi-nucleotide variants
11 months ago by amy__ ▴ 240
0
votes
0
replies
1.7k
views
Comment: Comment: Help with the new nomenclature of multi-nucleotide variants
11 months ago by amy__ ▴ 240
0
votes
13
replies
1.7k
views
Help with the new nomenclature of multi-nucleotide variants
bam igv multinucleotide
11 months ago by amy__ ▴ 240
0
votes
0
replies
1.1k
views
Comment: Comment: If the mane transcript isn't available should you use the canonical transcript?
11 months ago by amy__ ▴ 240
2
votes
4
replies
1.1k
views
If the mane transcript isn't available should you use the canonical transcript?
ensembl mane gnomad canonical
11 months ago by amy__ ▴ 240
0
votes
0
replies
1.1k
views
Comment: Comment: If the mane transcript isn't available should you use the canonical transcript?
11 months ago by amy__ ▴ 240
0
votes
1
reply
546
views
LOFTEE flag on GnomAD - END_TRUNC
loftee gnomad
updated 12 months ago by 165k • written 12 months ago by ▴ 240
0
votes
1
reply
439
views
Extracting LOF variants and incidence from GnomAD for a list of genes
Gnomad LOF genes
updated 13 months ago by 4.5k • written 13 months ago by ▴ 240
1
vote
0
replies
1.3k
views
Comment: Comment: Genotypes in vcf files
14 months ago by amy__ ▴ 240
0
votes
0
replies
1.3k
views
Comment: Comment: Genotypes in vcf files
15 months ago by amy__ ▴ 240
0
votes
1
reply
1.3k
views
Comment: Comment: Genotypes in vcf files
15 months ago by amy__ ▴ 240
2
votes
6
replies
1.3k
views
Genotypes in vcf files
genotypes vcf
updated 14 months ago by 23k • written 15 months ago by ▴ 240
0
votes
0
replies
406
views
Filtering vcf by strand bias / annotating strand bias on
Vcf
updated 15 months ago by 44k • written 15 months ago by ▴ 240
0
votes
1
reply
540
views
How to find the most representative protein data base ID for your protein?
modelling protein database
updated 17 months ago by 149k • written 17 months ago by ▴ 240
2
votes
1
reply
1.1k
views
Answer: Answer: Why do the same genetic variants sometimes result in different amino acids in th
18 months ago by amy__ ▴ 240
0
votes
1
reply
737
views
Comment: Comment: Classification for low quality variant on IGV
18 months ago by amy__ ▴ 240
1
vote
3
replies
737
views
Classification for low quality variant on IGV
bam igv
updated 18 months ago by ★ 2.8k • written 18 months ago by ▴ 240
0
votes
0
replies
1.3k
views
Comment: Comment: IGV - is it possible to tell what allele a read is from?
19 months ago by amy__ ▴ 240
6
votes
2
replies
1.3k
views
IGV - is it possible to tell what allele a read is from?
WES reads IGV
19 months ago by amy__ ▴ 240
0
votes
0
replies
2.8k
views
Comment: Comment: Deepvariant variant calling by singularity
19 months ago by amy__ ▴ 240
0
votes
0
replies
900
views
Comment: Comment: With cutadapt, is it possible to completely trim reads to empty reads instead of
19 months ago by amy__ ▴ 240
0
votes
0
replies
668
views
Comment: Comment: Low coverage in specific exons of genes - sequencing errors?
19 months ago by amy__ ▴ 240
3
votes
1
reply
3.1k
views
Answer: Answer: Don't choose Novogene for your sequencing projects
19 months ago by amy__ ▴ 240
1
vote
2
replies
668
views
Low coverage in specific exons of genes - sequencing errors?
coverage
19 months ago by amy__ ▴ 240
0
votes
1
reply
2.8k
views
Comment: Comment: Deepvariant variant calling by singularity
19 months ago by amy__ ▴ 240
0
votes
1
reply
2.8k
views
Comment: Comment: Deepvariant variant calling by singularity
19 months ago by amy__ ▴ 240
2
votes
0
replies
2.3k
views
Comment: Comment: Exome alignment and preprocessing: When I perform an exome alignment, should I u
20 months ago by amy__ ▴ 240
2
votes
1
reply
2.3k
views
Answer: Answer: Exome alignment and preprocessing: When I perform an exome alignment, should I u
20 months ago by amy__ ▴ 240
0
votes
0
replies
1.1k
views
Comment: Comment: Difference between USCS exon coordinates and ensembl
20 months ago by amy__ ▴ 240
0
votes
1
reply
1.1k
views
Comment: Comment: Difference between USCS exon coordinates and ensembl
20 months ago by amy__ ▴ 240
1
vote
4
replies
1.1k
views
Difference between USCS exon coordinates and ensembl
exons Ensembl
20 months ago by amy__ ▴ 240
0
votes
0
replies
475
views
GC content of WES cohort
WES FASTQC GC-content
updated 21 months ago by 44k • written 21 months ago by ▴ 240
0
votes
0
replies
2.6k
views
Answer: Answer: How to calculate the coverage of list of genes in whole exome data
22 months ago by amy__ ▴ 240
1
vote
1
reply
641
views
Variant depth cut off - justification
VCF depth variant
updated 22 months ago by ★ 2.8k • written 22 months ago by ▴ 240
0
votes
1
reply
1.4k
views
Comment: Comment: Linux command to edit CHROM column in VCF file
2.0 years ago by amy__ ▴ 240
0
votes
0
replies
945
views
Comment: Comment: Is it possible to do bedtools multicov across the entire genome?
2.0 years ago by amy__ ▴ 240
4
votes
3
replies
945
views
Is it possible to do bedtools multicov across the entire genome?
bedtools
updated 20 months ago by 44k • written 2.0 years ago by ▴ 240
0
votes
0
replies
476
views
Haloplex HS - should you remove duplicates?
deduplicate Haloplex duplicates
2.0 years ago by amy__ ▴ 240
0
votes
1
reply
1.0k
views
Comment: Comment: liftover output column help
2.1 years ago by amy__ ▴ 240
3
votes
3
replies
1.0k
views
liftover output column help
liftover
updated 2.1 years ago by 165k • written 2.1 years ago by ▴ 240
126 results • Page 1 of 3
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