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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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A question about the missing or not observed alleles in PLINK datasets
PLINK
5 months ago by abedkurdi10 ▴ 190
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6
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888
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A question about genotyping rate
genotyping snps harmonizer array
5 months ago by abedkurdi10 ▴ 190
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888
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Comment: Comment: A question about genotyping rate
5 months ago by abedkurdi10 ▴ 190
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888
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Comment: Comment: A question about genotyping rate
5 months ago by abedkurdi10 ▴ 190
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1
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888
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Comment: Comment: A question about genotyping rate
5 months ago by abedkurdi10 ▴ 190
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729
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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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4
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729
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DESeq2 analysis using two featureCounts generated from different studies
RNA-seq DESeq2
7 months ago by abedkurdi10 ▴ 190
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419
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A question about GWENA R/Bioconductor package
proteomics wgcna gwena
16 months ago by abedkurdi10 ▴ 190
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5.7k
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Comment: Comment: Trouble setting "ident" argument in FindMarkers in Seurat
19 months ago by abedkurdi10 ▴ 190
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1.1k
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Comment: Comment: SNP downstream analysis
2.1 years ago by abedkurdi10 ▴ 190
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1.1k
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Comment: Comment: SRA dataset to Seurat Object
2.1 years ago by abedkurdi10 ▴ 190
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872
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Comment: Comment: HT-Seq, Gene ID appeared in Gene Name row
2.1 years ago by abedkurdi10 ▴ 190
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1.1k
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Comment: Comment: SRA dataset to Seurat Object
2.1 years ago by abedkurdi10 ▴ 190
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2.0k
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Comment: Comment: How to label gene ID on volcano plot?
2.1 years ago by abedkurdi10 ▴ 190
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706
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Answer: Answer: I have RAW Illumina Paired-end sequence in FASTQ format. Can someone please guid
2.1 years ago by abedkurdi10 ▴ 190
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2.0k
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Comment: Comment: How to label gene ID on volcano plot?
2.1 years ago by abedkurdi10 ▴ 190
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2.0k
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Comment: Comment: How to label gene ID on volcano plot?
2.1 years ago by abedkurdi10 ▴ 190
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1
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952
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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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0
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616
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Comment: Comment: Variant Annotation Integrator VCF File
2.2 years ago by abedkurdi10 ▴ 190
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612
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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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940
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Comment: Comment: gene ID RNAseq
2.2 years ago by abedkurdi10 ▴ 190
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0
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641
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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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641
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Answer: Answer: Find a position in IGV when variant is giving in the format gene_name 12345-1G>
2.2 years ago by abedkurdi10 ▴ 190
2
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0
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3.2k
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Answer: Answer: Seurat Dotplot _ How can I have different panels on my doplot?
2.2 years ago by abedkurdi10 ▴ 190
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1
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940
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Comment: Comment: gene ID RNAseq
2.2 years ago by abedkurdi10 ▴ 190
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0
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575
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Answer: Answer: Liftover bosTau6ToBosTau9
2.2 years ago by abedkurdi10 ▴ 190
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0
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506
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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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940
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Comment: Comment: gene ID RNAseq
2.2 years ago by abedkurdi10 ▴ 190
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0
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597
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Answer: Answer: Ligand Receptor Interaction Algorithm
2.2 years ago by abedkurdi10 ▴ 190
1
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1
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706
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Answer: Answer: Hard filtering variants
2.2 years ago by abedkurdi10 ▴ 190
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0
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647
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Answer: Answer: Filter SNPs within VCF / .ChromR object using a custom list of mouse ensembl id
2.2 years ago by abedkurdi10 ▴ 190
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0
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1.6k
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Comment: Comment: seurat dotplot issue
2.2 years ago by abedkurdi10 ▴ 190
1
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0
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561
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Answer: Answer: Heatmap in ggplot
2.2 years ago by abedkurdi10 ▴ 190
1
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0
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673
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Answer: Answer: eagle2 + minimac4 script for phasing and imputation
2.2 years ago by abedkurdi10 ▴ 190
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0
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761
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Comment: Comment: Data sets of WGS + disease phenotypes?
2.3 years ago by abedkurdi10 ▴ 190
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0
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605
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Answer: Answer: Single cell Sequencing
2.3 years ago by abedkurdi10 ▴ 190
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0
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946
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Comment: Comment: getting indexing files using hisat2-build
2.3 years ago by abedkurdi10 ▴ 190
1
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0
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1.1k
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Answer: Answer: SNP downstream analysis
2.3 years ago by abedkurdi10 ▴ 190
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0
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645
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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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1
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761
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Answer: Answer: Data sets of WGS + disease phenotypes?
2.3 years ago by abedkurdi10 ▴ 190
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0
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5.7k
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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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1.0k
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Answer: Answer: Where I can get pipeline for covid genome assembly?
2.3 years ago by abedkurdi10 ▴ 190
3
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0
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1.3k
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Answer: Answer: Downstream analysis of VCF file
2.3 years ago by abedkurdi10 ▴ 190
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1
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3.8k
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Answer: Answer: Seurat orig.ident
2.3 years ago by abedkurdi10 ▴ 190
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0
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5.5k
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Comment: Comment: Finding Subclusters in Seurat Clusters
2.5 years ago by abedkurdi10 ▴ 190
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