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Processing WES VCF for case control GWAS analysis
GWAS PLINK
updated 16 months ago by ▴ 520 • written 16 months ago by • 0
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1.4k
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Comment: Comment: ExomeDepth error in getBamCounts when adding a fasta reference
16 months ago by sonsunjirachote • 0
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1
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540
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Calling zero mapping quality variant
calling GATK variant
updated 19 months ago by ▴ 120 • written 19 months ago by • 0
0
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0
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829
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Enrichment map in python/ Pathway network by using python
network pathway-enrichment interaction
updated 18 months ago by 44k • written 20 months ago by • 0
0
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0
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627
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How to choose the right annotation from multiple annotation of single variant from snpeff result
snpeff
updated 21 months ago by 44k • written 21 months ago by • 0
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0
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48k
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Comment: Comment: How To Convert The Bed File To Ped File
2.1 years ago by sonsunjirachote • 0
0
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0
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412
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Annotate ethnic or ancestry in specific region by using VCF file from whole exome sequencing
VCF SNP Ethinic
2.1 years ago by sonsunjirachote • 0
3
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2
replies
1.4k
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Create violin plot with specific value label that corresponding to graph
R
updated 3.0 years ago by 146k • written 3.0 years ago by • 0
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1.4k
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Comment: Comment: Create violin plot with specific value label that corresponding to graph
3.0 years ago by sonsunjirachote • 0
0
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1
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1.7k
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Comment: Comment: Stringtie2 no reference transcript found
3.4 years ago by sonsunjirachote • 0
1
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3
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1.7k
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Stringtie2 no reference transcript found
alignment rna-seq nanopore stringtie samtools
updated 3.4 years ago by 146k • written 3.4 years ago by • 0
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2.2k
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Comment: Comment: What is the output of rna-seq alignment to reference transcriptome (FASTA+GTF) l
3.4 years ago by sonsunjirachote • 0
0
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0
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2.7k
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Comment: Comment: Nanopore data to gtf/gff file
3.4 years ago by sonsunjirachote • 0
0
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0
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2.2k
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Comment: Comment: What is the output of rna-seq alignment to reference transcriptome (FASTA+GTF) l
3.4 years ago by sonsunjirachote • 0
0
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6
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2.2k
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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 3.4 years ago by 146k • written 3.4 years ago by • 0
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3.3k
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Comment: Comment: How to calculate percent coverage of each read for nanopore
3.4 years ago by sonsunjirachote • 0
0
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1
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2.0k
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Comment: Comment: What codes do I use to generate gene cluster vectors with entrez gene id on clus
3.4 years ago by sonsunjirachote • 0
0
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1
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3.3k
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Comment: Comment: How to calculate percent coverage of each read for nanopore
3.4 years ago by sonsunjirachote • 0
0
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1
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3.3k
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Comment: Comment: How to calculate percent coverage of each read for nanopore
3.4 years ago by sonsunjirachote • 0
0
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1
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3.3k
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Comment: Comment: How to calculate percent coverage of each read for nanopore
3.4 years ago by sonsunjirachote • 0
0
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0
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3.3k
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Comment: Comment: How to calculate percent coverage of each read for nanopore
3.4 years ago by sonsunjirachote • 0
5
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13
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3.3k
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How to calculate percent coverage of each read for nanopore
alignment nanopore sequencing
3.4 years ago by sonsunjirachote • 0
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