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Comment: C: Rna-Seq Data Variant Calling
6.9 years ago by Kevin Blighe ★ 90k
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0
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16k
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Comment: C: Rna-Seq Data Variant Calling
6.9 years ago by Kevin Blighe ★ 90k
0
votes
0
replies
16k
views
Comment: C: Rna-Seq Data Variant Calling
6.9 years ago by Kevin Blighe ★ 90k
0
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0
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4.0k
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Comment: C: how to calling variants in RNAseq data from multiple samples?
6.9 years ago by Kevin Blighe ★ 90k
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0
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6.3k
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Comment: C: Call variant from RNA-Seq data using Haplotypecaller
6.9 years ago by Kevin Blighe ★ 90k
3
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0
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1.1k
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Answer: A: PPI networks in disease vs. healthy
6.9 years ago by Kevin Blighe ★ 90k
0
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1
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3.3k
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Comment: C: Retrieve list of kept SNP's after LD pruning
6.9 years ago by Kevin Blighe ★ 90k
2
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0
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1.8k
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Answer: A: DNA Microarray data from TCGA
6.9 years ago by Kevin Blighe ★ 90k
1
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0
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2.0k
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Answer: A: Star-fusion not finding reference fusion genes
6.9 years ago by Kevin Blighe ★ 90k
0
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1
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1.9k
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Comment: C: Why should the LD plot (LD heatmap) be created in control samples, not cases?
6.9 years ago by Kevin Blighe ★ 90k
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0
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9.9k
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Comment: C: Imputation of vcf file
6.9 years ago by Kevin Blighe ★ 90k
0
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0
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9.9k
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Comment: C: Imputation of vcf file
6.9 years ago by Kevin Blighe ★ 90k
0
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0
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3.2k
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Comment: C: Conversion of imputed output file from beagle 4.1 to vcf dosage format
6.9 years ago by Kevin Blighe ★ 90k
1
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1
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21k
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Comment: C: Issues installing bcl2fastq?
6.9 years ago by Kevin Blighe ★ 90k
0
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1
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9.9k
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Comment: C: Imputation of vcf file
6.9 years ago by Kevin Blighe ★ 90k
0
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1
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10k
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Comment: C: DESeq2 design formula: how to use the opposite interaction term?
6.9 years ago by Kevin Blighe ★ 90k
0
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0
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4.8k
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Comment: C: Different samples order in .ped and phynotype data files
6.9 years ago by Kevin Blighe ★ 90k
1
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0
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1.9k
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Comment: C: question about survival analysis
6.9 years ago by Kevin Blighe ★ 90k
1
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0
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12k
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Answer: A: Log2FC and p value
6.9 years ago by Kevin Blighe ★ 90k
0
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0
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3.1k
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Answer: A: Compare Microarray with RNA-Seq
6.9 years ago by Kevin Blighe ★ 90k
4
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1
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4.0k
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Answer: A: How to merge microarray and RNA-SEQ expression data for DEG analysis?
6.9 years ago by Kevin Blighe ★ 90k
1
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0
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4.7k
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Comment: C: PLINK assoc input: can it be two vcf files case/control?
6.9 years ago by Kevin Blighe ★ 90k
2
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1
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4.7k
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Comment: C: PLINK assoc input: can it be two vcf files case/control?
6.9 years ago by Kevin Blighe ★ 90k
0
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0
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1.9k
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Answer: A: question about survival analysis
6.9 years ago by Kevin Blighe ★ 90k
3
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1
reply
4.7k
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Answer: A: PLINK assoc input: can it be two vcf files case/control?
6.9 years ago by Kevin Blighe ★ 90k
1
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1
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1.4k
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Answer: A: Fusion sequence matching
6.9 years ago by Kevin Blighe ★ 90k
2
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1
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4.9k
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Answer: A: How to generate MAP file?
6.9 years ago by Kevin Blighe ★ 90k
1
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1
reply
1.8k
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Answer: A: How to construct GCN?
6.9 years ago by Kevin Blighe ★ 90k
0
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0
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1.5k
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Answer: A: HGMD procedure for novel mutation registration
6.9 years ago by Kevin Blighe ★ 90k
0
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1
reply
4.0k
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Comment: C: Normalizing RPPA data counts from TCGA
6.9 years ago by Kevin Blighe ★ 90k
0
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0
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3.2k
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Comment: C: Is linearity maintained in linear regression of RNA-Seq?
6.9 years ago by Kevin Blighe ★ 90k
4
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1
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3.2k
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Answer: Answer: Is linearity maintained in linear regression of RNA-Seq?
2.3 years ago by Kevin Blighe ★ 90k
0
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0
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25k
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Comment: C: Deconvolution Methods on RNA-Seq Data (Mixed cell types)
6.9 years ago by Kevin Blighe ★ 90k
1
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1
reply
2.6k
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Comment: C: How to identify dysregulated pathways using Support Vector machine (SVM)?
6.9 years ago by Kevin Blighe ★ 90k
5
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1
reply
8.3k
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Comment: Comment: How to calculate the Pearson correlation coefficients between a list of genes?
4.5 years ago by Kevin Blighe ★ 90k
0
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1
reply
4.0k
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Comment: C: Normalizing RPPA data counts from TCGA
6.9 years ago by Kevin Blighe ★ 90k
2
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1
reply
2.6k
views
Comment: C: How to identify dysregulated pathways using Support Vector machine (SVM)?
6.9 years ago by Kevin Blighe ★ 90k
2
votes
1
reply
2.6k
views
Comment: C: How to identify dysregulated pathways using Support Vector machine (SVM)?
6.9 years ago by Kevin Blighe ★ 90k
1
vote
1
reply
8.3k
views
Comment: C: How to calculate the Pearson correlation coefficients between a list of genes?
6.9 years ago by Kevin Blighe ★ 90k
2
votes
1
reply
2.6k
views
Comment: C: How to identify dysregulated pathways using Support Vector machine (SVM)?
6.9 years ago by Kevin Blighe ★ 90k
0
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2
replies
9.9k
views
Comment: C: Imputation of vcf file
6.9 years ago by Kevin Blighe ★ 90k
0
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2
replies
8.7k
views
Comment: C: Converting Microarray SNP data into VCF format
6.9 years ago by Kevin Blighe ★ 90k
0
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1
reply
8.7k
views
Comment: C: Converting Microarray SNP data into VCF format
6.9 years ago by Kevin Blighe ★ 90k
0
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1
reply
8.7k
views
Comment: C: Converting Microarray SNP data into VCF format
6.9 years ago by Kevin Blighe ★ 90k
0
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0
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3.0k
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Comment: C: Differential analysis with replicates using edgeR
6.9 years ago by Kevin Blighe ★ 90k
0
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1
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3.0k
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Comment: C: TCGA calling pipeline query
6.9 years ago by Kevin Blighe ★ 90k
1
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0
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1.1k
views
Answer: A: Estimating individual batch factors
6.9 years ago by Kevin Blighe ★ 90k
2
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1
reply
8.7k
views
Answer: A: Converting Microarray SNP data into VCF format
6.9 years ago by Kevin Blighe ★ 90k
1
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0
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2.6k
views
Answer: A: question about mutation data from TCGA
6.9 years ago by Kevin Blighe ★ 90k
0
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0
replies
1.4k
views
Comment: C: locuszoom software error
6.9 years ago by Kevin Blighe ★ 90k
10,067 results • Page 114 of 202
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