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Comment: Comment: A question about the missing or not observed alleles in PLINK datasets
13 months ago by abedkurdi10 ▴ 190
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2
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661
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A question about the missing or not observed alleles in PLINK datasets
PLINK
13 months ago by abedkurdi10 ▴ 190
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6
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1.3k
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A question about genotyping rate
genotyping snps harmonizer array
14 months ago by abedkurdi10 ▴ 190
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1.3k
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Comment: Comment: A question about genotyping rate
14 months ago by abedkurdi10 ▴ 190
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1.3k
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Comment: Comment: A question about genotyping rate
14 months ago by abedkurdi10 ▴ 190
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1.3k
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Comment: Comment: A question about genotyping rate
14 months ago by abedkurdi10 ▴ 190
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1.1k
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Comment: Comment: DESeq2 analysis using two featureCounts generated from different studies
15 months ago by abedkurdi10 ▴ 190
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4
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1.1k
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DESeq2 analysis using two featureCounts generated from different studies
RNA-seq DESeq2
15 months ago by abedkurdi10 ▴ 190
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500
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A question about GWENA R/Bioconductor package
proteomics wgcna gwena
2.1 years ago by abedkurdi10 ▴ 190
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8.1k
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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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1
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1.4k
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Comment: Comment: SNP downstream analysis
2.8 years ago by abedkurdi10 ▴ 190
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1.4k
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Comment: Comment: SRA dataset to Seurat Object
2.8 years ago by abedkurdi10 ▴ 190
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1
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1.1k
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Comment: Comment: HT-Seq, Gene ID appeared in Gene Name row
2.8 years ago by abedkurdi10 ▴ 190
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1
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1.4k
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Comment: Comment: SRA dataset to Seurat Object
2.8 years ago by abedkurdi10 ▴ 190
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2.5k
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Comment: Comment: How to label gene ID on volcano plot?
2.8 years ago by abedkurdi10 ▴ 190
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0
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832
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Answer: Answer: I have RAW Illumina Paired-end sequence in FASTQ format. Can someone please guid
2.8 years ago by abedkurdi10 ▴ 190
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1
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2.5k
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Comment: Comment: How to label gene ID on volcano plot?
2.8 years ago by abedkurdi10 ▴ 190
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1
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2.5k
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Comment: Comment: How to label gene ID on volcano plot?
2.8 years ago by abedkurdi10 ▴ 190
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1
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1.2k
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Comment: Comment: VariantsToTable not produce output file
2.9 years ago by abedkurdi10 ▴ 190
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1
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1.4k
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Comment: Comment: filter and annotate vcf file
2.9 years ago by abedkurdi10 ▴ 190
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0
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1.5k
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Comment: Comment: Existing tutorials using Docker to set up and run any type of NGS workflow?
2.9 years ago by abedkurdi10 ▴ 190
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0
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2.4k
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Comment: Comment: How can I download the VCF file of the 1000 genomes project with the population
2.9 years ago by abedkurdi10 ▴ 190
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0
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1.5k
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Comment: Comment: Existing tutorials using Docker to set up and run any type of NGS workflow?
2.9 years ago by abedkurdi10 ▴ 190
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0
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752
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Comment: Comment: Variant Annotation Integrator VCF File
2.9 years ago by abedkurdi10 ▴ 190
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0
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732
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Comment: Comment: convert unmapped bam to fastqs and preserve tag
2.9 years ago by abedkurdi10 ▴ 190
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0
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1.2k
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Comment: Comment: gene ID RNAseq
2.9 years ago by abedkurdi10 ▴ 190
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0
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837
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Comment: Comment: Find a position in IGV when variant is giving in the format gene_name 12345-1G>
2.9 years ago by abedkurdi10 ▴ 190
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1
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837
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Answer: Answer: Find a position in IGV when variant is giving in the format gene_name 12345-1G>
2.9 years ago by abedkurdi10 ▴ 190
2
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0
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4.2k
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Answer: Answer: Seurat Dotplot _ How can I have different panels on my doplot?
2.9 years ago by abedkurdi10 ▴ 190
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1
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1.2k
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Comment: Comment: gene ID RNAseq
2.9 years ago by abedkurdi10 ▴ 190
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0
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737
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Answer: Answer: Liftover bosTau6ToBosTau9
2.9 years ago by abedkurdi10 ▴ 190
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0
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633
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Comment: Comment: VEP and future analysis
2.9 years ago by abedkurdi10 ▴ 190
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1
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1.2k
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Comment: Comment: gene ID RNAseq
2.9 years ago by abedkurdi10 ▴ 190
1
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0
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736
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Answer: Answer: Ligand Receptor Interaction Algorithm
2.9 years ago by abedkurdi10 ▴ 190
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1
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876
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Answer: Answer: Hard filtering variants
2.9 years ago by abedkurdi10 ▴ 190
1
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0
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820
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Answer: Answer: Filter SNPs within VCF / .ChromR object using a custom list of mouse ensembl id
2.9 years ago by abedkurdi10 ▴ 190
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0
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2.0k
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Comment: Comment: seurat dotplot issue
2.9 years ago by abedkurdi10 ▴ 190
1
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0
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720
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Answer: Answer: Heatmap in ggplot
2.9 years ago by abedkurdi10 ▴ 190
1
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0
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869
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Answer: Answer: eagle2 + minimac4 script for phasing and imputation
2.9 years ago by abedkurdi10 ▴ 190
0
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0
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955
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Comment: Comment: Data sets of WGS + disease phenotypes?
3.0 years ago by abedkurdi10 ▴ 190
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0
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722
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Answer: Answer: Single cell Sequencing
3.0 years ago by abedkurdi10 ▴ 190
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0
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1.1k
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Comment: Comment: getting indexing files using hisat2-build
3.0 years ago by abedkurdi10 ▴ 190
1
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0
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1.4k
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Answer: Answer: SNP downstream analysis
3.0 years ago by abedkurdi10 ▴ 190
0
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0
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789
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Comment: Comment: Rsubread: Aligning multiple single and paired-end reads from multiple files (lan
3.0 years ago by abedkurdi10 ▴ 190
0
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1
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955
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Answer: Answer: Data sets of WGS + disease phenotypes?
3.0 years ago by abedkurdi10 ▴ 190
0
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0
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8.1k
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Comment: Comment: Trouble setting "ident" argument in FindMarkers in Seurat
3.0 years ago by abedkurdi10 ▴ 190
0
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1
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1.3k
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Answer: Answer: Where I can get pipeline for covid genome assembly?
3.0 years ago by abedkurdi10 ▴ 190
3
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0
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1.6k
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Answer: Answer: Downstream analysis of VCF file
3.0 years ago by abedkurdi10 ▴ 190
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1
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5.0k
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Answer: Answer: Seurat orig.ident
3.0 years ago by abedkurdi10 ▴ 190
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0
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6.1k
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Comment: Comment: Finding Subclusters in Seurat Clusters
3.2 years ago by abedkurdi10 ▴ 190
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