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Comment: Ensemble Neural Network - Stacking ensemble neural network accuracy is significa
6 weeks ago by
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Comment:
Comment: Ensemble Neural Network - Stacking ensemble neural network accuracy is significa
6 weeks ago by
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442
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Comment: Variant calling in tumor/normal pairs is calling heterozygous positions
6 weeks ago by
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1
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442
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Comment:
Comment: Variant calling in tumor/normal pairs is calling heterozygous positions
7 weeks ago by
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442
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Comment:
Comment: Variant calling in tumor/normal pairs is calling heterozygous positions
7 weeks ago by
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0
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1
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629
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Comment:
Comment: Snakemake - pipeline shut down without error
6 months ago by
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1
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1
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545
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Comment:
Comment: human_variation_vcf
6 months ago by
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1
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545
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Comment:
Comment: human_variation_vcf
6 months ago by
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0
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1.9k
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Comment:
Comment: RNA-Seq mutation calling without germline data
6 months ago by
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1.9k
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Comment:
Comment: RNA-Seq mutation calling without germline data
6 months ago by
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811
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Comment:
Comment: RNA-seq anlaysis > coding region vs. non coding region
8 months ago by
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427
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Comment:
Comment: VCF file GL field confusion
9 months ago by
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2
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578
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Comment:
Comment: dbSNP download and merge to my data
10 months ago by
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3.6k
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Comment:
Comment: Python script to query GeneCards to get EntrezID, symbol from Ensembl geneID
11 months ago by
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891
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Comment:
Comment: Pearson correlation between Gene and clinical parameters
13 months ago by
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0
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891
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Comment:
Comment: Pearson correlation between Gene and clinical parameters
13 months ago by
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0
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614
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Comment:
Comment: seaborn dispersion graph
13 months ago by
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0
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669
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Comment:
Comment: How to show that correlation from one method is more significant than other meth
14 months ago by
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0
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1
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669
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Comment:
Comment: How to show that correlation from one method is more significant than other meth
14 months ago by
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0
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1
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720
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Comment:
Comment: Snakemake paralellize
14 months ago by
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0
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0
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951
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Comment:
Comment: How to find SNP locations in assemblies other than hg38
14 months ago by
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0
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1.0k
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Comment:
Comment: RNA-seq deconvolution algorithm that takes into account weight of marker gene
15 months ago by
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1.0k
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Comment:
Comment: RNA-seq deconvolution algorithm that takes into account weight of marker gene
15 months ago by
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1
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784
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Comment:
Comment: How to identify regions of similarity/identity that are exclusive for a group wi
16 months ago by
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1
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978
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Comment:
Comment: GO, KEGG, GSEA analysis with ~5 DEGs
16 months ago by
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1
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1.9k
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Comment:
Comment: Data preparation for a ML model
17 months ago by
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1
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1.9k
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Comment:
Comment: Data preparation for a ML model
17 months ago by
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★ 1.6k
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1
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1.2k
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Comment:
Comment: How to change from gene_id to GeneID/EntrezID using R
19 months ago by
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1
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1.5k
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Comment:
Comment: STAR mapping two pass mode for multiple samples with split steps or one step ?
19 months ago by
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0
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988
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Comment:
Comment: Can we use exon- counts to calculate coverage?
19 months ago by
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1
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1.1k
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Comment:
Comment: Integrated analysis of RNA-seq datasets
20 months ago by
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★ 1.6k
1
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0
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1.2k
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Comment:
Comment: Keplen Meyer Curve Dropping to zero
21 months ago by
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1
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1.2k
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Comment:
Comment: Keplen Meyer Curve Dropping to zero
21 months ago by
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★ 1.6k
0
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1
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687
views
Comment:
Comment: python 'gnomAD_DB'
21 months ago by
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★ 1.6k
1
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0
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791
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Comment:
Comment: Estimating sample size from bulk RNAseq data
22 months ago by
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1
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2.9k
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Comment:
Comment: Typical percentage of multimapping reads in human rna-seq?
22 months ago by
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0
votes
0
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1.6k
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Comment:
Comment: TPM normalization but library size isn't equal to 1 million
22 months ago by
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1
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0
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1.4k
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Comment:
Comment: rank SNPs after elastic net modeling
22 months ago by
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1
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1.4k
views
Comment:
Comment: rank SNPs after elastic net modeling
22 months ago by
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★ 1.6k
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1
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1.4k
views
Comment:
Comment: rank SNPs after elastic net modeling
22 months ago by
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★ 1.6k
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1
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1.3k
views
Comment:
Comment: Segmentation fault Biopython pairwise alignment
23 months ago by
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0
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0
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1.5k
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Comment:
Comment: Inquiry Regarding Somatic Analysis and Normal Sample Requirement
23 months ago by
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★ 1.6k
0
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1
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1.5k
views
Comment:
Comment: Inquiry Regarding Somatic Analysis and Normal Sample Requirement
23 months ago by
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★ 1.6k
1
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1
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1.5k
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Comment:
Comment: How to get the gene ID
23 months ago by
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★ 1.6k
2
votes
0
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972
views
Comment:
Comment: How do I use the new human pangenome reference to discover SNV and SV.
23 months ago by
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0
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2.9k
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Comment:
Comment: How to calculate the coverage of list of genes in whole exome data
2.0 years ago by
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0
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1
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2.9k
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Comment:
Comment: How to calculate the coverage of list of genes in whole exome data
2.0 years ago by
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★ 1.6k
0
votes
1
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2.9k
views
Comment:
Comment: How to calculate the coverage of list of genes in whole exome data
2.0 years ago by
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★ 1.6k
0
votes
1
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1.9k
views
Comment:
Comment: gatk4 download issue
2.0 years ago by
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★ 1.6k
0
votes
0
replies
2.5k
views
Comment:
Comment: Allele Frequency >0.5 for cancer somatic mutations?
2.0 years ago by
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