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Comment: Comment: A question about the missing or not observed alleles in PLINK datasets
5 months ago by abedkurdi10 ▴ 190
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943
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Comment: Comment: A question about genotyping rate
6 months ago by abedkurdi10 ▴ 190
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1
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943
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Comment: Comment: A question about genotyping rate
6 months ago by abedkurdi10 ▴ 190
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1
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943
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Comment: Comment: A question about genotyping rate
6 months ago by abedkurdi10 ▴ 190
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771
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Comment: Comment: DESeq2 analysis using two featureCounts generated from different studies
7 months ago by abedkurdi10 ▴ 190
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6.0k
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Comment: Comment: Trouble setting "ident" argument in FindMarkers in Seurat
20 months ago by abedkurdi10 ▴ 190
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1.2k
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Comment: Comment: SNP downstream analysis
2.1 years ago by abedkurdi10 ▴ 190
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1.2k
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Comment: Comment: SRA dataset to Seurat Object
2.1 years ago by abedkurdi10 ▴ 190
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895
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Comment: Comment: HT-Seq, Gene ID appeared in Gene Name row
2.2 years ago by abedkurdi10 ▴ 190
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1.2k
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Comment: Comment: SRA dataset to Seurat Object
2.2 years ago by abedkurdi10 ▴ 190
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2.1k
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Comment: Comment: How to label gene ID on volcano plot?
2.2 years ago by abedkurdi10 ▴ 190
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2.1k
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Comment: Comment: How to label gene ID on volcano plot?
2.2 years ago by abedkurdi10 ▴ 190
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2.1k
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Comment: Comment: How to label gene ID on volcano plot?
2.2 years ago by abedkurdi10 ▴ 190
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1
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970
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Comment: Comment: VariantsToTable not produce output file
2.2 years ago by abedkurdi10 ▴ 190
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1
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1.1k
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Comment: Comment: filter and annotate vcf file
2.2 years ago by abedkurdi10 ▴ 190
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1.2k
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Comment: Comment: Existing tutorials using Docker to set up and run any type of NGS workflow?
2.2 years ago by abedkurdi10 ▴ 190
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1.9k
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Comment: Comment: How can I download the VCF file of the 1000 genomes project with the population
2.2 years ago by abedkurdi10 ▴ 190
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1.2k
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Comment: Comment: Existing tutorials using Docker to set up and run any type of NGS workflow?
2.2 years ago by abedkurdi10 ▴ 190
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630
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Comment: Comment: Variant Annotation Integrator VCF File
2.2 years ago by abedkurdi10 ▴ 190
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629
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Comment: Comment: convert unmapped bam to fastqs and preserve tag
2.2 years ago by abedkurdi10 ▴ 190
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964
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Comment: Comment: gene ID RNAseq
2.2 years ago by abedkurdi10 ▴ 190
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656
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Comment: Comment: Find a position in IGV when variant is giving in the format gene_name 12345-1G>
2.2 years ago by abedkurdi10 ▴ 190
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1
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964
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Comment: Comment: gene ID RNAseq
2.2 years ago by abedkurdi10 ▴ 190
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518
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Comment: Comment: VEP and future analysis
2.2 years ago by abedkurdi10 ▴ 190
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1
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964
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Comment: Comment: gene ID RNAseq
2.2 years ago by abedkurdi10 ▴ 190
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1.7k
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Comment: Comment: seurat dotplot issue
2.2 years ago by abedkurdi10 ▴ 190
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777
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Comment: Comment: Data sets of WGS + disease phenotypes?
2.3 years ago by abedkurdi10 ▴ 190
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963
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Comment: Comment: getting indexing files using hisat2-build
2.3 years ago by abedkurdi10 ▴ 190
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663
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Comment: Comment: Rsubread: Aligning multiple single and paired-end reads from multiple files (lan
2.3 years ago by abedkurdi10 ▴ 190
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6.0k
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Comment: Comment: Trouble setting "ident" argument in FindMarkers in Seurat
2.3 years ago by abedkurdi10 ▴ 190
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5.6k
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Comment: Comment: Finding Subclusters in Seurat Clusters
2.6 years ago by abedkurdi10 ▴ 190
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29k
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Comment: Comment: Batch correction in DESeq2
2.6 years ago by abedkurdi10 ▴ 190
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1
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5.6k
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Comment: Comment: Finding Subclusters in Seurat Clusters
2.6 years ago by abedkurdi10 ▴ 190
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961
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Comment: C: RNA-seq Infer experiment wrong strandeness information
3.9 years ago by abedkurdi10 ▴ 190
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2.6k
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Comment: C: Interval list for GATK tool Haplotype Caller
3.9 years ago by abedkurdi10 ▴ 190
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1
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3.7k
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Comment: C: Conversion of Vep.vcf to MAF format?
4.0 years ago by abedkurdi10 ▴ 190
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3.7k
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Comment: C: Conversion of Vep.vcf to MAF format?
4.0 years ago by abedkurdi10 ▴ 190
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1.2k
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Comment: C: Bigwig circular plot
4.1 years ago by abedkurdi10 ▴ 190
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2.1k
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Comment: C: Replace the bases with N for the sites with evidence of a SNP
4.9 years ago by abedkurdi10 ▴ 190
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1
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2.1k
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Comment: C: Replace the bases with N for the sites with evidence of a SNP
4.9 years ago by abedkurdi10 ▴ 190
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1
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2.1k
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Comment: A: Replace the bases with N for the sites with evidence of a SNP
4.9 years ago by abedkurdi10 ▴ 190
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2
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2.3k
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Comment: C: Optimal number of samples needed to detect a variant from panel sequencing
7.2 years ago by abedkurdi10 ▴ 190
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1
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2.3k
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Comment: C: Optimal number of samples needed to detect a variant from panel sequencing
7.2 years ago by abedkurdi10 ▴ 190
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2.3k
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Comment: C: Optimal number of samples needed to detect a variant from panel sequencing
7.2 years ago by abedkurdi10 ▴ 190
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2.2k
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Comment: C: Statistics on BED files
7.3 years ago by abedkurdi10 ▴ 190
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1
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3.9k
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Comment: C: Thresholds to filter out variants from vcf file
7.5 years ago by abedkurdi10 ▴ 190
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1
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3.9k
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Comment: C: Thresholds to filter out variants from vcf file
7.5 years ago by abedkurdi10 ▴ 190
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4.6k
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Comment: C: VCF file re-header
7.5 years ago by abedkurdi10 ▴ 190
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4.6k
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Comment: C: VCF file re-header
7.5 years ago by abedkurdi10 ▴ 190
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4.4k
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Comment: C: Clinical significance explanation
7.5 years ago by abedkurdi10 ▴ 190
53 results • Page 1 of 2
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