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Comment: C: Multiple testing correction issue
5.0 years ago by CY ▴ 750
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0
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2.1k
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Comment: C: Multiple testing correction issue
5.0 years ago by CY ▴ 750
0
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2
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2.1k
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Comment: C: Multiple testing correction issue
5.0 years ago by CY ▴ 750
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1
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2.1k
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Comment: C: Multiple testing correction issue
5.0 years ago by CY ▴ 750
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1
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1.7k
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Comment: C: Can we get absolute abundance of TCR using TCR-Seq?
5.2 years ago by CY ▴ 750
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1
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1.7k
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Comment: C: Can we get absolute abundance of TCR using TCR-Seq?
5.2 years ago by CY ▴ 750
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2.4k
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Comment: C: Is linearity maintained in linear regression of RNA-Seq?
5.3 years ago by CY ▴ 750
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1
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2.4k
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Comment: C: Is linearity maintained in linear regression of RNA-Seq?
5.3 years ago by CY ▴ 750
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1
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21k
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Comment: C: Deconvolution Methods on RNA-Seq Data (Mixed cell types)
5.3 years ago by CY ▴ 750
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6.9k
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Comment: C: Log-transformed RNA-Seq data and linear regression
5.3 years ago by CY ▴ 750
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0
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6.9k
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Comment: C: Log-transformed RNA-Seq data and linear regression
5.3 years ago by CY ▴ 750
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2
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3.8k
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Comment: C: Why use LASSO / elastic net in survival regression?
5.4 years ago by CY ▴ 750
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1
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869
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Comment: C: Can remote, but same type, tissue be used as RNA-Seq normal control for tumor st
5.4 years ago by CY ▴ 750
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1
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4.3k
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Comment: C: Why NMF for mutation signature analysis
5.4 years ago by CY ▴ 750
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1
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4.3k
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Comment: C: Why NMF for mutation signature analysis
5.4 years ago by CY ▴ 750
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0
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4.3k
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Comment: C: Why NMF for mutation signature analysis
5.4 years ago by CY ▴ 750
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0
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982
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Comment: C: Transcriptomic profile fluctuation between different time point
5.5 years ago by CY ▴ 750
1
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0
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982
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Comment: C: Transcriptomic profile fluctuation between different time point
5.5 years ago by CY ▴ 750
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1
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982
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Comment: C: Transcriptomic profile fluctuation between different time point
5.5 years ago by CY ▴ 750
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1
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1.1k
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Comment: C: Gene expression distribution (non-DE and DE)
5.5 years ago by CY ▴ 750
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1
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1.1k
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Comment: C: Gene expression distribution (non-DE and DE)
5.5 years ago by CY ▴ 750
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1
reply
1.4k
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Comment: C: Low VAF (around 7%) mutated gene prevalent in cancer patient (3/4), driver?
5.5 years ago by CY ▴ 750
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1
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1.4k
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Comment: C: Low VAF (around 7%) mutated gene prevalent in cancer patient (3/4), driver?
5.5 years ago by CY ▴ 750
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0
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6.4k
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Comment: C: What kind of distribution to you expect to see for RNA-Seq expression levels?
5.5 years ago by CY ▴ 750
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0
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1.4k
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Comment: C: Would different enrichment tools result differently by defining pathway differen
5.5 years ago by CY ▴ 750
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1
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1.4k
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Comment: C: Difference between gene set enrichment and pathway enrichment
5.6 years ago by CY ▴ 750
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0
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1.7k
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Comment: C: Any tools to estimate the relative abundance of immune cell in tumor
5.6 years ago by CY ▴ 750
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1
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12k
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Comment: C: Interesting bioinformatics blogs (2017 edition)
5.8 years ago by CY ▴ 750
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5.0k
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Comment: C: Your Favorite Bioinformatics Blogs (October 2011)
5.8 years ago by CY ▴ 750
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0
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1.2k
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Comment: C: Why VarScan always get more somatic variants than other caller
5.8 years ago by CY ▴ 750
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1
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1.2k
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Comment: C: Why VarScan always get more somatic variants than other caller
5.8 years ago by CY ▴ 750
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1
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1.2k
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Comment: C: Why VarScan always get more somatic variants than other caller
5.8 years ago by CY ▴ 750
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1
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3.9k
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Comment: C: Immunotherapy tools for predicting binding affinity between TCR and epitode
5.9 years ago by CY ▴ 750
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1
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1.9k
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Comment: C: SciClone: Why cluster in non-CN neutral region considering it infers only on CN
5.9 years ago by CY ▴ 750
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0
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2.1k
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Comment: C: SciClone: Which Variant to Which Clone
5.9 years ago by CY ▴ 750
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0
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4.0k
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Comment: C: STAR-HT-Seq/featureCount got much more gene expression count than RSEM did
5.9 years ago by CY ▴ 750
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1
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4.0k
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Comment: C: STAR-HT-Seq/featureCount got much more gene expression count than RSEM did
5.9 years ago by CY ▴ 750
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1
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3.2k
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Comment: C: SciClone not numeric error
5.9 years ago by CY ▴ 750
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1
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18k
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Comment: C: why PCA for RNA-Seq but tSNE for scRNA-seq?
5.9 years ago by CY ▴ 750
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0
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1.9k
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Comment: C: Inconsistency of allele depth in BAM and VCF
6.0 years ago by CY ▴ 750
0
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0
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5.0k
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Comment: C: Lack of consensus between NGS & Sanger sequencing on indels/mutations
6.1 years ago by CY ▴ 750
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1
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5.0k
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Comment: C: Lack of consensus between NGS & Sanger sequencing on indels/mutations
6.1 years ago by CY ▴ 750
0
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1
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2.1k
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Comment: C: call somatic CNV from cfDNA with normal control
6.1 years ago by CY ▴ 750
0
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1
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1.7k
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Comment: C: During GO / pathway enrichment analysis, should we exclude genes not expressed i
6.1 years ago by CY ▴ 750
0
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1
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1.7k
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Comment: C: During GO / pathway enrichment analysis, should we exclude genes not expressed i
6.1 years ago by CY ▴ 750
0
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1
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1.7k
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Comment: C: During GO / pathway enrichment analysis, should we exclude genes not expressed i
6.1 years ago by CY ▴ 750
0
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1
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1.2k
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Comment: C: one sample from pool shows low quality at the end, why?
6.1 years ago by CY ▴ 750
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0
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1.2k
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Comment: C: one sample from pool shows low quality at the end, why?
6.1 years ago by CY ▴ 750
0
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0
replies
1.2k
views
Comment: C: one sample from pool shows low quality at the end, why?
6.1 years ago by CY ▴ 750
0
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1
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2.1k
views
Comment: C: call somatic CNV from cfDNA with normal control
6.1 years ago by CY ▴ 750
148 results • Page 2 of 3
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