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Comment: Comment: VEP filtering query
3 months ago by prasundutta87 ▴ 660
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Comment: Comment: VEP filtering query
3 months ago by prasundutta87 ▴ 660
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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
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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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1.2k
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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
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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
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671
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Comment: Comment: I need help with a methyl array data analysis
11 months ago by prasundutta87 ▴ 660
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607
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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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840
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Comment: Comment: Very high coverage Nanopore alignment Hg38
13 months ago by prasundutta87 ▴ 660
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971
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Comment: Comment: VCF file filter for breakpoints
13 months ago by prasundutta87 ▴ 660
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971
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Comment: Comment: VCF file filter for breakpoints
13 months ago by prasundutta87 ▴ 660
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Comment: Comment: Sample Level Filtering During GATK Germline Short Variant Discovery
14 months ago by prasundutta87 ▴ 660
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876
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Comment: Comment: alternate allele frequency and minor allele frequency
18 months ago by prasundutta87 ▴ 660
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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
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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
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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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4.4k
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Comment: Comment: RNA Seq data network analysis
2.2 years ago by prasundutta87 ▴ 660
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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
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2.0k
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Comment: Comment: Variant annotation using VEP
2.5 years ago by prasundutta87 ▴ 660
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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
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2.0k
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Comment: Comment: Variant annotation using VEP
2.5 years ago by prasundutta87 ▴ 660
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2.0k
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Comment: Comment: Variant annotation using VEP
2.5 years ago by prasundutta87 ▴ 660
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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
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1.4k
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Comment: Comment: VEP chromosome name query
2.9 years ago by prasundutta87 ▴ 660
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1.4k
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Comment: Comment: VEP chromosome name query
2.9 years ago by prasundutta87 ▴ 660
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1
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1.4k
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Comment: Comment: VEP chromosome name query
2.9 years ago by prasundutta87 ▴ 660
1
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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
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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
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1.4k
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Comment: Comment: Masking sites in a vcf file
2.9 years ago by prasundutta87 ▴ 660
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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
2
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1
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2.5k
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Comment: Comment: Flagstats and multiqc
2.9 years ago by prasundutta87 ▴ 660
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2.7k
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Comment: Comment: how to get iDs in VCF file?
2.9 years ago by prasundutta87 ▴ 660
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1.0k
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Comment: Comment: Mutation hunting in 100 exome samples
3.0 years ago by prasundutta87 ▴ 660
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2.7k
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Comment: Comment: Comparing two variant files
3.0 years ago by prasundutta87 ▴ 660
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0
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2.7k
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Comment: Comment: Comparing two variant files
3.0 years ago by prasundutta87 ▴ 660
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1
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2.7k
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Comment: Comment: Comparing two variant files
3.0 years ago by prasundutta87 ▴ 660
1
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1
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2.2k
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Comment: Comment: How do I filter a multi-individual BCF file for genotype probabilities
3.0 years ago by prasundutta87 ▴ 660
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4.6k
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Comment: Comment: how to use the samtools filtering expression ?
3.0 years ago by prasundutta87 ▴ 660
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2
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4.6k
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Comment: Comment: how to use the samtools filtering expression ?
3.0 years ago by prasundutta87 ▴ 660
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2.0k
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Comment: Comment: Allele Specific Expression (ASE) from RNA seq data
3.0 years ago by prasundutta87 ▴ 660
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1
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2.0k
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Comment: Comment: Allele Specific Expression (ASE) from RNA seq data
3.0 years ago by prasundutta87 ▴ 660
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1.7k
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Comment: Comment: remove unmapped reads on a specific chromosome only
3.1 years ago by prasundutta87 ▴ 660
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1.3k
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Comment: Comment: Finding transcriptome coverage of genome
3.1 years ago by prasundutta87 ▴ 660
0
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0
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914
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Comment: Comment: Multiple Transctipr ID (NM ) from MyVariantInfo
3.1 years ago by prasundutta87 ▴ 660
2
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1
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1.3k
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Comment: Comment: TiTv ratio
3.1 years ago by prasundutta87 ▴ 660
2
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1.4k
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Comment: Comment: Picard and GaTK HaplotypeCaller
3.1 years ago by prasundutta87 ▴ 660
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0
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723
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Comment: C: How to keep the individual read depth with bcftools call?
3.1 years ago by prasundutta87 ▴ 660
0
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1
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7.5k
views
Comment: C: how to remove duplicates with picard
3.2 years ago by prasundutta87 ▴ 660
159 results • Page 1 of 4
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