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2
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2.7k
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Answer: A: How to start Gene Analysis?
9.0 years ago by Amitm ★ 2.3k
1
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0
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2.7k
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Answer: A: RNA Seq coverage
9.0 years ago by Amitm ★ 2.3k
1
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1
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2.0k
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Answer: A: Capillary sequencing data analysis
9.0 years ago by Amitm ★ 2.3k
0
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1
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2.5k
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Answer: A: Infer loss of heterozygosity from SNP variant frequencies
9.0 years ago by Amitm ★ 2.3k
0
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1
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2.8k
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Answer: A: Assembled TCGA dataset download
9.0 years ago by Amitm ★ 2.3k
1
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0
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1.3k
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Answer: A: how to check which probesets belong to which transcript?
9.0 years ago by Amitm ★ 2.3k
2
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2
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5.4k
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Answer: A: how to understand gene fusion and how to call gene fusion ?
9.0 years ago by Amitm ★ 2.3k
1
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0
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2.3k
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Answer: A: Annotation: From GO to IPS
9.0 years ago by Amitm ★ 2.3k
1
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1
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3.9k
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Answer: A: How to find exact allele frequency for the SNP/indel variants ?
9.0 years ago by Amitm ★ 2.3k
0
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1
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4.3k
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Answer: A: Filtering reads aligned to specific chromosome
9.1 years ago by Amitm ★ 2.3k
0
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0
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3.1k
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Answer: A: TCGA RNAseq normal and tumor samples problem
9.1 years ago by Amitm ★ 2.3k
1
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0
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1.5k
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Answer: A: Interreplicate statistics for microarray data?
9.1 years ago by Amitm ★ 2.3k
4
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0
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8.8k
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Answer: A: Variant caller for low frequency variants
9.1 years ago by Amitm ★ 2.3k
0
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2
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5.4k
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Answer: A: issues with the precalculated lookup in Interproscan-5.17-56.0
9.1 years ago by Amitm ★ 2.3k
2
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1
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6.2k
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Answer: C: Machine Learning - RNAseq
9.1 years ago by Amitm ★ 2.3k
1
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0
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2.6k
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Answer: Answer: Source for Normals for Bladder Cancer RNA-Seq
updated 3.0 years ago by 45k • written 9.1 years ago by ★ 2.3k
1
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0
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1.9k
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Answer: Answer: Please suggest a suitable tool for GO annotation of a plant de novo assembled tr
updated 2.7 years ago by 45k • written 9.1 years ago by ★ 2.3k
0
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0
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1.9k
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Answer: A: mapping known epitopes in a protein sequcence
9.1 years ago by Amitm ★ 2.3k
2
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1
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7.8k
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Answer: Answer: How to calculate enrichment P-value?
updated 2.7 years ago by 45k • written 9.1 years ago by ★ 2.3k
0
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0
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1.9k
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Answer: Answer: Regarding Human Exon Variant Reference
updated 2.7 years ago by 45k • written 9.1 years ago by ★ 2.3k
1
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1
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4.8k
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Answer: A: What's wrong with this sample? (kmers found by FastQC of RNA-Seq)
9.2 years ago by Amitm ★ 2.3k
0
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2
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4.1k
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Answer: A: Somatic allele frequency from TCGA in non-coding DNA
9.2 years ago by Amitm ★ 2.3k
3
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2
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4.1k
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Answer: A: Somatic allele frequency from TCGA
9.2 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
9.2 years ago by Amitm ★ 2.3k
1
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0
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4.0k
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Answer: C: microarray meta- analysis
9.2 years ago by Amitm ★ 2.3k
10
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2
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6.3k
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Answer: A: How to decide the quality of RNA-seq analysis
9.2 years ago by Amitm ★ 2.3k
1
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1
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2.5k
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Answer: A: Binning BED file and counting antisense / sense reads
9.2 years ago by Amitm ★ 2.3k
1
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0
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1.9k
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Answer: A: new gene discovery
9.2 years ago by Amitm ★ 2.3k
1
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1
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5.4k
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Answer: A: Somatic mutations from RNA-Seq data of tumor vs. normal
9.2 years ago by Amitm ★ 2.3k
1
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0
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8.3k
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Answer: A: How should I normalized RNA-seq data to draw the gene expression time series cur
9.8 years ago by Amitm ★ 2.3k
2
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0
replies
40k
views
Answer: A: Best Way To Normalize Rna-Seq Data For Expression Profiling
9.8 years ago by Amitm ★ 2.3k
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