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3.2k
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Comment: C: analyzing RNAseq data in cytoscape
8.8 years ago by Amitm ★ 2.3k
1
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0
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4.2k
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Comment: C: Reference and dbSNP incompatibility issue (MuTect2)
8.8 years ago by Amitm ★ 2.3k
0
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1
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1.1k
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Comment: C: RNAseq large differences in mapping
8.8 years ago by Amitm ★ 2.3k
1
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0
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5.5k
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Comment: C: Something better than GSEA?
8.8 years ago by Amitm ★ 2.3k
0
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0
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5.4k
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Comment: C: alignment rate in bowtie2
8.8 years ago by Amitm ★ 2.3k
1
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1
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5.4k
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Comment: C: alignment rate in bowtie2
8.8 years ago by Amitm ★ 2.3k
0
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0
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2.4k
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Comment: C: Which tool for pathway analysis ?
8.8 years ago by Amitm ★ 2.3k
0
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0
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8.2k
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Comment: C: RefSeq Ids(NM*, NR*) to ensemble transcript Ids (ENST*)
8.9 years ago by Amitm ★ 2.3k
0
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0
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2.0k
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Comment: C: What NGS courses would you like us to prepare for 2016? (one week left)
8.9 years ago by Amitm ★ 2.3k
1
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0
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2.7k
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Comment: C: RNA-Seq quantitation for human, paired end vs single end, strand specific or not
8.9 years ago by Amitm ★ 2.3k
0
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1
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3.7k
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Comment: C: Somatic allele frequency from TCGA in non-coding DNA
8.9 years ago by Amitm ★ 2.3k
1
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1
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3.7k
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Comment: C: Somatic allele frequency from TCGA in non-coding DNA
8.9 years ago by Amitm ★ 2.3k
0
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2
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3.7k
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Answer: A: Somatic allele frequency from TCGA in non-coding DNA
8.9 years ago by Amitm ★ 2.3k
3
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2
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3.7k
views
Answer: A: Somatic allele frequency from TCGA
8.9 years ago by Amitm ★ 2.3k
0
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0
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2.3k
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Comment: C: Rna-Seq alternative splicing analysis under limited conditions: possible?
8.9 years ago by Amitm ★ 2.3k
0
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0
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26k
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Comment: C: Kmer Content in FastQC failed
8.9 years ago by Amitm ★ 2.3k
18
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1
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26k
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Answer: A: Kmer Content in FastQC failed
8.9 years ago by Amitm ★ 2.3k
1
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0
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3.9k
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Answer: C: microarray meta- analysis
8.9 years ago by Amitm ★ 2.3k
1
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1
reply
5.8k
views
Comment: C: How to decide the quality of RNA-seq analysis
8.9 years ago by Amitm ★ 2.3k
10
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2
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5.8k
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Answer: A: How to decide the quality of RNA-seq analysis
8.9 years ago by Amitm ★ 2.3k
1
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1
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2.4k
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Answer: A: Binning BED file and counting antisense / sense reads
8.9 years ago by Amitm ★ 2.3k
0
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1
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3.7k
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Comment: C: Removing PCR primers in targeted sequencing with nested amplicons
8.9 years ago by Amitm ★ 2.3k
0
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1
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3.7k
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Comment: C: Removing PCR primers in targeted sequencing with nested amplicons
8.9 years ago by Amitm ★ 2.3k
1
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0
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1.8k
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Answer: A: new gene discovery
8.9 years ago by Amitm ★ 2.3k
1
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1
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5.3k
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Answer: A: Somatic mutations from RNA-Seq data of tumor vs. normal
8.9 years ago by Amitm ★ 2.3k
0
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0
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5.4k
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Comment: C: How to calculate read depth and coverage for whole exome sequencing?
8.9 years ago by Amitm ★ 2.3k
4
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1
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2.5k
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Comment: C: Assemble fully overlapping reads into contigs that may have several clones
8.9 years ago by Amitm ★ 2.3k
0
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0
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2.5k
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Comment: C: checking many somatic mutations in IGV
8.9 years ago by Amitm ★ 2.3k
1
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0
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8.2k
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Answer: A: How should I normalized RNA-seq data to draw the gene expression time series cur
9.5 years ago by Amitm ★ 2.3k
2
votes
0
replies
40k
views
Answer: A: Best Way To Normalize Rna-Seq Data For Expression Profiling
9.5 years ago by Amitm ★ 2.3k
280 results • Page 6 of 6
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