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Comment: Snakemake - pipeline shut down without error
26 days ago by
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Comment: human_variation_vcf
28 days ago by
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Comment: human_variation_vcf
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Comment: RNA-Seq mutation calling without germline data
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Comment: RNA-Seq mutation calling without germline data
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Comment: RNA-seq anlaysis > coding region vs. non coding region
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Comment: VCF file GL field confusion
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Comment: dbSNP download and merge to my data
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Comment: Python script to query GeneCards to get EntrezID, symbol from Ensembl geneID
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Comment: Pearson correlation between Gene and clinical parameters
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Comment: Pearson correlation between Gene and clinical parameters
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Comment: seaborn dispersion graph
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Comment: How to show that correlation from one method is more significant than other meth
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Comment: How to show that correlation from one method is more significant than other meth
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Comment: Snakemake paralellize
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680
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Comment: How to find SNP locations in assemblies other than hg38
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Comment: RNA-seq deconvolution algorithm that takes into account weight of marker gene
10 months ago by
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Comment: RNA-seq deconvolution algorithm that takes into account weight of marker gene
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Comment: How to identify regions of similarity/identity that are exclusive for a group wi
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717
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Comment: GO, KEGG, GSEA analysis with ~5 DEGs
11 months ago by
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Comment: Data preparation for a ML model
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Comment: Data preparation for a ML model
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930
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Comment: How to change from gene_id to GeneID/EntrezID using R
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Comment: STAR mapping two pass mode for multiple samples with split steps or one step ?
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788
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Comment: Can we use exon- counts to calculate coverage?
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Comment: Integrated analysis of RNA-seq datasets
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Comment: Keplen Meyer Curve Dropping to zero
15 months ago by
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909
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Comment: Keplen Meyer Curve Dropping to zero
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Comment: python 'gnomAD_DB'
15 months ago by
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Comment: Estimating sample size from bulk RNAseq data
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Comment: Typical percentage of multimapping reads in human rna-seq?
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Comment: TPM normalization but library size isn't equal to 1 million
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Comment: rank SNPs after elastic net modeling
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Comment: rank SNPs after elastic net modeling
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Comment: rank SNPs after elastic net modeling
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Comment: Segmentation fault Biopython pairwise alignment
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Comment: Inquiry Regarding Somatic Analysis and Normal Sample Requirement
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Comment: Inquiry Regarding Somatic Analysis and Normal Sample Requirement
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Comment: How to get the gene ID
18 months ago by
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Comment: How do I use the new human pangenome reference to discover SNV and SV.
18 months ago by
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Comment: How to calculate the coverage of list of genes in whole exome data
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Comment: How to calculate the coverage of list of genes in whole exome data
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Comment: How to calculate the coverage of list of genes in whole exome data
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Comment: gatk4 download issue
19 months ago by
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Comment: Allele Frequency >0.5 for cancer somatic mutations?
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Comment: How do you find two genes exclusively expressed in a given tissue / cell type?
19 months ago by
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Comment: Advice about building a computational project to investigate porphyrin’s roles i
19 months ago by
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Comment: How do you find two genes exclusively expressed in a given tissue / cell type?
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Comment: How to make "Custom annotation File" for GO analysis using TOPgo
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Comment: Alignment REST API
19 months ago by
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