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Comment: C: analyzing RNAseq data in cytoscape
9.8 years ago by Amitm ★ 2.3k
1
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0
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5.0k
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Comment: C: Reference and dbSNP incompatibility issue (MuTect2)
9.8 years ago by Amitm ★ 2.3k
0
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1
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1.3k
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Comment: C: RNAseq large differences in mapping
9.8 years ago by Amitm ★ 2.3k
1
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0
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6.8k
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Comment: C: Something better than GSEA?
9.8 years ago by Amitm ★ 2.3k
0
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0
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6.2k
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Comment: C: alignment rate in bowtie2
9.8 years ago by Amitm ★ 2.3k
1
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1
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6.2k
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Comment: C: alignment rate in bowtie2
9.8 years ago by Amitm ★ 2.3k
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0
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2.6k
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Comment: C: Which tool for pathway analysis ?
9.8 years ago by Amitm ★ 2.3k
0
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0
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9.8k
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Comment: C: RefSeq Ids(NM*, NR*) to ensemble transcript Ids (ENST*)
9.8 years ago by Amitm ★ 2.3k
0
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0
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2.3k
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Comment: C: What NGS courses would you like us to prepare for 2016? (one week left)
9.8 years ago by Amitm ★ 2.3k
1
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0
replies
2.9k
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Comment: C: RNA-Seq quantitation for human, paired end vs single end, strand specific or not
9.8 years ago by Amitm ★ 2.3k
0
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1
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4.9k
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Comment: C: Somatic allele frequency from TCGA in non-coding DNA
9.8 years ago by Amitm ★ 2.3k
1
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1
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4.9k
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Comment: C: Somatic allele frequency from TCGA in non-coding DNA
9.8 years ago by Amitm ★ 2.3k
0
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2
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4.9k
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Answer: A: Somatic allele frequency from TCGA in non-coding DNA
9.8 years ago by Amitm ★ 2.3k
3
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2
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4.9k
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Answer: A: Somatic allele frequency from TCGA
9.8 years ago by Amitm ★ 2.3k
0
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0
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3.1k
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Comment: C: Rna-Seq alternative splicing analysis under limited conditions: possible?
9.8 years ago by Amitm ★ 2.3k
0
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0
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27k
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Comment: C: Kmer Content in FastQC failed
9.8 years ago by Amitm ★ 2.3k
18
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1
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27k
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Answer: A: Kmer Content in FastQC failed
9.8 years ago by Amitm ★ 2.3k
1
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0
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4.3k
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Answer: C: microarray meta- analysis
9.8 years ago by Amitm ★ 2.3k
1
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1
reply
7.3k
views
Comment: C: How to decide the quality of RNA-seq analysis
9.8 years ago by Amitm ★ 2.3k
10
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2
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7.3k
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Answer: A: How to decide the quality of RNA-seq analysis
9.8 years ago by Amitm ★ 2.3k
1
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1
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2.8k
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Answer: A: Binning BED file and counting antisense / sense reads
9.8 years ago by Amitm ★ 2.3k
0
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1
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4.3k
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Comment: C: Removing PCR primers in targeted sequencing with nested amplicons
9.8 years ago by Amitm ★ 2.3k
0
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1
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4.3k
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Comment: C: Removing PCR primers in targeted sequencing with nested amplicons
9.8 years ago by Amitm ★ 2.3k
1
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0
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2.2k
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Answer: A: new gene discovery
9.8 years ago by Amitm ★ 2.3k
1
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1
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5.9k
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Answer: A: Somatic mutations from RNA-Seq data of tumor vs. normal
9.8 years ago by Amitm ★ 2.3k
0
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0
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5.7k
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Comment: C: How to calculate read depth and coverage for whole exome sequencing?
9.8 years ago by Amitm ★ 2.3k
4
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1
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2.9k
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Comment: C: Assemble fully overlapping reads into contigs that may have several clones
9.8 years ago by Amitm ★ 2.3k
0
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0
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2.8k
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Comment: C: checking many somatic mutations in IGV
9.8 years ago by Amitm ★ 2.3k
1
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0
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8.8k
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Answer: A: How should I normalized RNA-seq data to draw the gene expression time series cur
10.4 years ago by Amitm ★ 2.3k
2
votes
0
replies
41k
views
Answer: A: Best Way To Normalize Rna-Seq Data For Expression Profiling
10.4 years ago by Amitm ★ 2.3k
280 results • Page 6 of 6
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