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Comment: Comment: Should we cite sed / awk in papers?
24 days ago by amy__ ▴ 250
4
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5
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428
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Should we cite sed / awk in papers?
sed awk
updated 24 days ago by 87k • written 24 days ago by ▴ 250
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701
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Comment: Comment: What companies do you recommend for targeted sequencing?
5 months ago by amy__ ▴ 250
4
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4
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701
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Forum: What companies do you recommend for targeted sequencing?
Targeted-sequencing
5 months ago by amy__ ▴ 250
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0
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701
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Comment: Comment: What companies do you recommend for targeted sequencing?
6 months ago by amy__ ▴ 250
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1
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567
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Comment: Comment: Germline variant - should it be seen in the somatic vcf?
6 months ago by amy__ ▴ 250
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3
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567
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Germline variant - should it be seen in the somatic vcf?
vcf somatic
updated 6 months ago by 45k • written 6 months ago by ▴ 250
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0
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311
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Advice on telling if two SNPs are on the same haplotype
ldpair halplotype co-occurance gnomad snp
12 months ago by amy__ ▴ 250
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0
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1.8k
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Comment: Comment: Help with the new nomenclature of multi-nucleotide variants
12 months ago by amy__ ▴ 250
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1
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1.8k
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Comment: Comment: Help with the new nomenclature of multi-nucleotide variants
12 months ago by amy__ ▴ 250
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1
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1.8k
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Comment: Comment: Help with the new nomenclature of multi-nucleotide variants
12 months ago by amy__ ▴ 250
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1
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1.8k
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Comment: Comment: Help with the new nomenclature of multi-nucleotide variants
12 months ago by amy__ ▴ 250
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1
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1.8k
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Comment: Comment: Help with the new nomenclature of multi-nucleotide variants
12 months ago by amy__ ▴ 250
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0
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1.8k
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Comment: Comment: Help with the new nomenclature of multi-nucleotide variants
12 months ago by amy__ ▴ 250
0
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13
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1.8k
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Help with the new nomenclature of multi-nucleotide variants
bam igv multinucleotide
12 months ago by amy__ ▴ 250
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0
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1.2k
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Comment: Comment: If the mane transcript isn't available should you use the canonical transcript?
12 months ago by amy__ ▴ 250
2
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4
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1.2k
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If the mane transcript isn't available should you use the canonical transcript?
ensembl mane gnomad canonical
12 months ago by amy__ ▴ 250
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0
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1.2k
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Comment: Comment: If the mane transcript isn't available should you use the canonical transcript?
12 months ago by amy__ ▴ 250
0
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1
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574
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LOFTEE flag on GnomAD - END_TRUNC
loftee gnomad
updated 13 months ago by 165k • written 13 months ago by ▴ 250
0
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1
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461
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Extracting LOF variants and incidence from GnomAD for a list of genes
Gnomad LOF genes
updated 14 months ago by 4.5k • written 14 months ago by ▴ 250
1
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0
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1.4k
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Comment: Comment: Genotypes in vcf files
15 months ago by amy__ ▴ 250
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0
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1.4k
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Comment: Comment: Genotypes in vcf files
15 months ago by amy__ ▴ 250
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1
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1.4k
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Comment: Comment: Genotypes in vcf files
15 months ago by amy__ ▴ 250
2
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6
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1.4k
views
Genotypes in vcf files
genotypes vcf
updated 15 months ago by 23k • written 15 months ago by ▴ 250
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0
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423
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Filtering vcf by strand bias / annotating strand bias on
Vcf
updated 16 months ago by 45k • written 16 months ago by ▴ 250
0
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1
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567
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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 ▴ 250
2
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1
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1.1k
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Answer: Answer: Why do the same genetic variants sometimes result in different amino acids in th
19 months ago by amy__ ▴ 250
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1
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770
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Comment: Comment: Classification for low quality variant on IGV
19 months ago by amy__ ▴ 250
1
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3
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770
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Classification for low quality variant on IGV
bam igv
updated 19 months ago by ★ 2.9k • written 19 months ago by ▴ 250
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0
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1.4k
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Comment: Comment: IGV - is it possible to tell what allele a read is from?
20 months ago by amy__ ▴ 250
6
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2
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1.4k
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IGV - is it possible to tell what allele a read is from?
WES reads IGV
20 months ago by amy__ ▴ 250
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0
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2.9k
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Comment: Comment: Deepvariant variant calling by singularity
20 months ago by amy__ ▴ 250
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0
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938
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Comment: Comment: With cutadapt, is it possible to completely trim reads to empty reads instead of
20 months ago by amy__ ▴ 250
0
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0
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695
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Comment: Comment: Low coverage in specific exons of genes - sequencing errors?
20 months ago by amy__ ▴ 250
3
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1
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3.3k
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Answer: Answer: Don't choose Novogene for your sequencing projects
20 months ago by amy__ ▴ 250
1
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2
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695
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Low coverage in specific exons of genes - sequencing errors?
coverage
20 months ago by amy__ ▴ 250
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1
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2.9k
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Comment: Comment: Deepvariant variant calling by singularity
20 months ago by amy__ ▴ 250
0
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1
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2.9k
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Comment: Comment: Deepvariant variant calling by singularity
20 months ago by amy__ ▴ 250
2
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0
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2.4k
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Comment: Comment: Exome alignment and preprocessing: When I perform an exome alignment, should I u
21 months ago by amy__ ▴ 250
2
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1
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2.4k
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Answer: Answer: Exome alignment and preprocessing: When I perform an exome alignment, should I u
21 months ago by amy__ ▴ 250
0
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0
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1.2k
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Comment: Comment: Difference between USCS exon coordinates and ensembl
21 months ago by amy__ ▴ 250
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1
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1.2k
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Comment: Comment: Difference between USCS exon coordinates and ensembl
21 months ago by amy__ ▴ 250
1
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4
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1.2k
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Difference between USCS exon coordinates and ensembl
exons Ensembl
21 months ago by amy__ ▴ 250
0
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0
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498
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GC content of WES cohort
WES FASTQC GC-content
updated 22 months ago by 45k • written 22 months ago by ▴ 250
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0
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2.7k
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Answer: Answer: How to calculate the coverage of list of genes in whole exome data
23 months ago by amy__ ▴ 250
1
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1
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668
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Variant depth cut off - justification
VCF depth variant
updated 23 months ago by ★ 2.9k • written 23 months ago by ▴ 250
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1
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1.4k
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Comment: Comment: Linux command to edit CHROM column in VCF file
2.1 years ago by amy__ ▴ 250
0
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0
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972
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Comment: Comment: Is it possible to do bedtools multicov across the entire genome?
2.1 years ago by amy__ ▴ 250
4
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3
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972
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Is it possible to do bedtools multicov across the entire genome?
bedtools
updated 21 months ago by 45k • written 2.1 years ago by ▴ 250
0
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0
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497
views
Haloplex HS - should you remove duplicates?
deduplicate Haloplex duplicates
2.1 years ago by amy__ ▴ 250
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