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160
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Advice on telling if two SNPs are on the same haplotype
ldpair halplotype co-occurance gnomad snp
5 weeks ago by amy__ ▴ 160
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0
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859
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Comment: Comment: Help with the new nomenclature of multi-nucleotide variants
6 weeks ago by amy__ ▴ 160
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1
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859
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Comment: Comment: Help with the new nomenclature of multi-nucleotide variants
6 weeks ago by amy__ ▴ 160
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1
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859
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Comment: Comment: Help with the new nomenclature of multi-nucleotide variants
6 weeks ago by amy__ ▴ 160
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1
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859
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Comment: Comment: Help with the new nomenclature of multi-nucleotide variants
6 weeks ago by amy__ ▴ 160
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1
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859
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Comment: Comment: Help with the new nomenclature of multi-nucleotide variants
6 weeks ago by amy__ ▴ 160
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0
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859
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Comment: Comment: Help with the new nomenclature of multi-nucleotide variants
6 weeks ago by amy__ ▴ 160
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13
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859
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Help with the new nomenclature of multi-nucleotide variants
bam igv multinucleotide
6 weeks ago by amy__ ▴ 160
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571
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Comment: Comment: If the mane transcript isn't available should you use the canonical transcript?
7 weeks ago by amy__ ▴ 160
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4
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571
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If the mane transcript isn't available should you use the canonical transcript?
ensembl mane gnomad canonical
7 weeks ago by amy__ ▴ 160
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0
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571
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Comment: Comment: If the mane transcript isn't available should you use the canonical transcript?
8 weeks ago by amy__ ▴ 160
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1
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274
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LOFTEE flag on GnomAD - END_TRUNC
loftee gnomad
updated 10 weeks ago by 161k • written 10 weeks ago by ▴ 160
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1
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207
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Extracting LOF variants and incidence from GnomAD for a list of genes
Gnomad LOF genes
updated 3 months ago by 4.2k • written 3 months ago by ▴ 160
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808
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Comment: Comment: Genotypes in vcf files
5 months ago by amy__ ▴ 160
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0
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808
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Comment: Comment: Genotypes in vcf files
5 months ago by amy__ ▴ 160
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1
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808
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Comment: Comment: Genotypes in vcf files
5 months ago by amy__ ▴ 160
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6
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808
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Genotypes in vcf files
genotypes vcf
updated 5 months ago by 22k • written 5 months ago by ▴ 160
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305
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Filtering vcf by strand bias / annotating strand bias on
Vcf
updated 5 months ago by 43k • written 5 months ago by ▴ 160
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1
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380
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How to find the most representative protein data base ID for your protein?
modelling protein database
updated 7 months ago by 141k • written 7 months ago by ▴ 160
2
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1
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798
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Answer: Answer: Why do the same genetic variants sometimes result in different amino acids in th
8 months ago by amy__ ▴ 160
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1
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502
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Comment: Comment: Classification for low quality variant on IGV
8 months ago by amy__ ▴ 160
1
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3
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502
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Classification for low quality variant on IGV
bam igv
updated 8 months ago by ★ 1.9k • written 8 months ago by ▴ 160
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848
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Comment: Comment: IGV - is it possible to tell what allele a read is from?
9 months ago by amy__ ▴ 160
6
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2
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848
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IGV - is it possible to tell what allele a read is from?
WES reads IGV
9 months ago by amy__ ▴ 160
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0
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1.7k
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Comment: Comment: Deepvariant variant calling by singularity
9 months ago by amy__ ▴ 160
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612
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Comment: Comment: With cutadapt, is it possible to completely trim reads to empty reads instead of
9 months ago by amy__ ▴ 160
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0
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497
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Comment: Comment: Low coverage in specific exons of genes - sequencing errors?
9 months ago by amy__ ▴ 160
3
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1
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1.9k
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Answer: Answer: Don't choose Novogene for your sequencing projects
9 months ago by amy__ ▴ 160
1
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2
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497
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Low coverage in specific exons of genes - sequencing errors?
coverage
9 months ago by amy__ ▴ 160
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1
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1.7k
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Comment: Comment: Deepvariant variant calling by singularity
9 months ago by amy__ ▴ 160
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1
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1.7k
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Comment: Comment: Deepvariant variant calling by singularity
9 months ago by amy__ ▴ 160
2
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0
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1.7k
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Comment: Comment: Exome alignment and preprocessing: When I perform an exome alignment, should I u
10 months ago by amy__ ▴ 160
2
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1
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1.7k
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Answer: Answer: Exome alignment and preprocessing: When I perform an exome alignment, should I u
10 months ago by amy__ ▴ 160
0
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0
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854
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Comment: Comment: Difference between USCS exon coordinates and ensembl
10 months ago by amy__ ▴ 160
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1
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854
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Comment: Comment: Difference between USCS exon coordinates and ensembl
10 months ago by amy__ ▴ 160
0
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4
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854
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Difference between USCS exon coordinates and ensembl
exons Ensembl
10 months ago by amy__ ▴ 160
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0
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340
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GC content of WES cohort
WES FASTQC GC-content
updated 11 months ago by 43k • written 11 months ago by ▴ 160
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1.7k
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Answer: Answer: How to calculate the coverage of list of genes in whole exome data
12 months ago by amy__ ▴ 160
1
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1
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475
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Variant depth cut off - justification
VCF depth variant
updated 12 months ago by ★ 1.9k • written 12 months ago by ▴ 160
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1
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1.0k
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Comment: Comment: Linux command to edit CHROM column in VCF file
14 months ago by amy__ ▴ 160
0
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0
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677
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Comment: Comment: Is it possible to do bedtools multicov across the entire genome?
14 months ago by amy__ ▴ 160
4
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3
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677
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Is it possible to do bedtools multicov across the entire genome?
bedtools
updated 10 months ago by 43k • written 14 months ago by ▴ 160
0
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0
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320
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Haloplex HS - should you remove duplicates?
deduplicate Haloplex duplicates
15 months ago by amy__ ▴ 160
0
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1
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742
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Comment: Comment: liftover output column help
15 months ago by amy__ ▴ 160
3
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3
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742
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liftover output column help
liftover
updated 15 months ago by 161k • written 15 months ago by ▴ 160
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1
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1.5k
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Comment: Comment: Vep results for a protein
17 months ago by amy__ ▴ 160
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2
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1.5k
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Answer: Answer: Vep results for a protein
17 months ago by amy__ ▴ 160
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1
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2.7k
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Comment: Comment: Understanding the VCF files
17 months ago by amy__ ▴ 160
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1
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2.7k
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Comment: Comment: Understanding the VCF files
17 months ago by amy__ ▴ 160
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0
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288
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GQ score - what do the numbers mean? How can this be interpreted?
vcf GQ
18 months ago by amy__ ▴ 160
121 results • Page 1 of 3
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