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Processing WES VCF for case control GWAS analysis
GWAS PLINK
updated 4 days ago by ▴ 360 • written 4 days ago by • 0
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0
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908
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Comment: Comment: ExomeDepth error in getBamCounts when adding a fasta reference
11 days ago by sonsunjirachote • 0
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1
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241
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Calling zero mapping quality variant
calling GATK variant
updated 3 months ago by ▴ 120 • written 3 months ago by • 0
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0
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287
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Enrichment map in python/ Pathway network by using python
network pathway-enrichment interaction
updated 11 weeks ago by 39k • written 4 months ago by • 0
0
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0
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274
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How to choose the right annotation from multiple annotation of single variant from snpeff result
snpeff
updated 5 months ago by 39k • written 5 months ago by • 0
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0
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44k
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Comment: Comment: How To Convert The Bed File To Ped File
9 months ago by sonsunjirachote • 0
0
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0
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213
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Annotate ethnic or ancestry in specific region by using VCF file from whole exome sequencing
VCF SNP Ethinic
9 months ago by sonsunjirachote • 0
3
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2
replies
862
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Create violin plot with specific value label that corresponding to graph
R
updated 20 months ago by 129k • written 20 months ago by • 0
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862
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Comment: Comment: Create violin plot with specific value label that corresponding to graph
20 months ago by sonsunjirachote • 0
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1
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1.0k
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Comment: Comment: Stringtie2 no reference transcript found
2.1 years ago by sonsunjirachote • 0
1
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3
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1.0k
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Stringtie2 no reference transcript found
alignment rna-seq nanopore stringtie samtools
updated 2.1 years ago by 129k • written 2.1 years ago by • 0
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1.3k
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Comment: Comment: What is the output of rna-seq alignment to reference transcriptome (FASTA+GTF) l
2.1 years ago by sonsunjirachote • 0
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0
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2.0k
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Comment: Comment: Nanopore data to gtf/gff file
2.1 years ago by sonsunjirachote • 0
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0
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1.3k
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Comment: Comment: What is the output of rna-seq alignment to reference transcriptome (FASTA+GTF) l
2.1 years ago by sonsunjirachote • 0
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6
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1.3k
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What is the output of rna-seq alignment to reference transcriptome (FASTA+GTF) look like in SAM format?
RNA-seq aligment nanopore
updated 2.1 years ago by 129k • written 2.1 years ago by • 0
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2.4k
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Comment: Comment: How to calculate percent coverage of each read for nanopore
2.1 years ago by sonsunjirachote • 0
0
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1
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1.3k
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Comment: Comment: What codes do I use to generate gene cluster vectors with entrez gene id on clus
2.1 years ago by sonsunjirachote • 0
0
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1
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2.4k
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Comment: Comment: How to calculate percent coverage of each read for nanopore
2.1 years ago by sonsunjirachote • 0
0
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1
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2.4k
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Comment: Comment: How to calculate percent coverage of each read for nanopore
2.1 years ago by sonsunjirachote • 0
0
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1
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2.4k
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Comment: Comment: How to calculate percent coverage of each read for nanopore
2.1 years ago by sonsunjirachote • 0
0
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0
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2.4k
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Comment: Comment: How to calculate percent coverage of each read for nanopore
2.1 years ago by sonsunjirachote • 0
5
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13
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2.4k
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How to calculate percent coverage of each read for nanopore
alignment nanopore sequencing
2.1 years ago by sonsunjirachote • 0
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