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Comment: Comment: VEP filtering query
3 months ago by prasundutta87 ▴ 660
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540
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Comment: Comment: VEP filtering query
3 months ago by prasundutta87 ▴ 660
2
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4
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540
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VEP filtering query
ensembl-vep
3 months ago by prasundutta87 ▴ 660
0
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1
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1.7k
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Comment: Comment: Which minimap2 parameters to set while performing mapping to avoid such mismatch
8 months ago by prasundutta87 ▴ 660
1
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0
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1.2k
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Comment: Comment: Coverage histogram query
8 months ago by prasundutta87 ▴ 660
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1
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1.2k
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Comment: Comment: Coverage histogram query
8 months ago by prasundutta87 ▴ 660
0
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1
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1.2k
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Comment: Comment: Coverage histogram query
8 months ago by prasundutta87 ▴ 660
0
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0
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1.2k
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Comment: Comment: Coverage histogram query
8 months ago by prasundutta87 ▴ 660
0
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1
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1.2k
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Comment: Comment: Coverage histogram query
8 months ago by prasundutta87 ▴ 660
1
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10
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1.2k
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Coverage histogram query
Alignment
8 months ago by prasundutta87 ▴ 660
0
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1
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671
views
Comment: Comment: I need help with a methyl array data analysis
11 months ago by prasundutta87 ▴ 660
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0
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606
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Comment: Comment: best practice to choose AF threshold based on population number
13 months ago by prasundutta87 ▴ 660
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2
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606
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best practice to choose AF threshold based on population number
VCF AF allele-frequency
13 months ago by prasundutta87 ▴ 660
0
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0
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839
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Comment: Comment: Very high coverage Nanopore alignment Hg38
13 months ago by prasundutta87 ▴ 660
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0
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971
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Comment: Comment: VCF file filter for breakpoints
13 months ago by prasundutta87 ▴ 660
1
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1
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971
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Comment: Comment: VCF file filter for breakpoints
13 months ago by prasundutta87 ▴ 660
0
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0
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987
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Comment: Comment: Sample Level Filtering During GATK Germline Short Variant Discovery
14 months ago by prasundutta87 ▴ 660
0
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0
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326
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snpeff annotation query
snpeff structural-variation VCF
updated 14 months ago by 43k • written 14 months ago by ▴ 660
0
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0
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874
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Comment: Comment: alternate allele frequency and minor allele frequency
18 months ago by prasundutta87 ▴ 660
0
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2
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874
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alternate allele frequency and minor allele frequency
rare common SNV SV VCF
18 months ago by prasundutta87 ▴ 660
0
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0
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904
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Answer: Answer: How to parse the output file of snpEFF
20 months ago by prasundutta87 ▴ 660
2
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0
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11k
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Comment: Comment: Correct way to calculate VAF (Variant allele fraction) from a VCF file
20 months ago by prasundutta87 ▴ 660
1
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2
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11k
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Comment: Comment: Correct way to calculate VAF (Variant allele fraction) from a VCF file
20 months ago by prasundutta87 ▴ 660
4
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11
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11k
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Correct way to calculate VAF (Variant allele fraction) from a VCF file
VCF snp
20 months ago by prasundutta87 ▴ 660
0
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0
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300
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Tool for mode of inheritance based filtering for structural variants
StructuralVariants genotypes SNVs trio modeOfInheritance
2.1 years ago by prasundutta87 ▴ 660
0
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1
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1.0k
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Comment: Comment: How to run fastqc for 500 raw sequence reads (100 single end and 400 paired end
2.1 years ago by prasundutta87 ▴ 660
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0
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4.4k
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Comment: Comment: RNA Seq data network analysis
2.2 years ago by prasundutta87 ▴ 660
2
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2
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2.9k
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EPIC methylation manifest GRch38 query
methylation coordinates EPIC bedgraph CpG
updated 2.3 years ago by ▴ 10 • written 3.9 years ago by ▴ 660
0
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0
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421
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query on filtering/dropping samples based on total reads (yield)
paired-end fastq Illumina
2.4 years ago by prasundutta87 ▴ 660
0
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0
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1.4k
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Comment: Comment: EPIC array data - How to find the total number of genes in the array?
2.5 years ago by prasundutta87 ▴ 660
0
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1
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1.4k
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Answer: Answer: EPIC array data - How to find the total number of genes in the array?
2.5 years ago by prasundutta87 ▴ 660
0
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0
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2.0k
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Comment: Comment: Variant annotation using VEP
2.5 years ago by prasundutta87 ▴ 660
0
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1
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2.0k
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Comment: Comment: Variant annotation using VEP
2.5 years ago by prasundutta87 ▴ 660
0
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1
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2.0k
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Comment: Comment: Variant annotation using VEP
2.5 years ago by prasundutta87 ▴ 660
0
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1
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2.0k
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Comment: Comment: Variant annotation using VEP
2.5 years ago by prasundutta87 ▴ 660
0
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1
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2.0k
views
Answer: Answer: Variant annotation using VEP
2.5 years ago by prasundutta87 ▴ 660
0
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0
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577
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Answer: Answer: calculation of gene coverage
2.5 years ago by prasundutta87 ▴ 660
0
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1
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591
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Structural variation nomenclature ambiguity
Structural_Variation
updated 2.6 years ago by ▴ 520 • written 2.6 years ago by ▴ 660
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0
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1.1k
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Comment: Comment: Annotate Structural variants with population specific allele frequency values
2.6 years ago by prasundutta87 ▴ 660
0
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2
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1.1k
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Annotate Structural variants with population specific allele frequency values
allele Structural_variation VEP frequency VCF
2.6 years ago by prasundutta87 ▴ 660
1
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1
reply
2.1k
views
Answer: Answer: Extract CDS from maker gff
2.8 years ago by prasundutta87 ▴ 660
0
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0
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1.4k
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Comment: Comment: VEP chromosome name query
2.9 years ago by prasundutta87 ▴ 660
3
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6
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1.4k
views
VEP chromosome name query
ensembl VCF annotation VEP
2.9 years ago by prasundutta87 ▴ 660
0
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0
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1.4k
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Comment: Comment: VEP chromosome name query
2.9 years ago by prasundutta87 ▴ 660
0
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1
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1.4k
views
Comment: Comment: VEP chromosome name query
2.9 years ago by prasundutta87 ▴ 660
1
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0
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638
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Comment: Comment: How to calculate the *necessary* sequencing depth for a SNP
2.9 years ago by prasundutta87 ▴ 660
0
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0
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517
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About Structural variation genotypes
variants Structural-variants variant-calling genotypes
updated 6 months ago by 43k • written 2.9 years ago by ▴ 660
0
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1
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1.7k
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Comment: Comment: Core Dumped - STAR mapping
2.9 years ago by prasundutta87 ▴ 660
1
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1
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1.4k
views
Comment: Comment: Masking sites in a vcf file
2.9 years ago by prasundutta87 ▴ 660
0
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1
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1.7k
views
Comment: Comment: Core Dumped - STAR mapping
2.9 years ago by prasundutta87 ▴ 660
260 results • Page 1 of 6
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