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2
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Answer: A: How to start Gene Analysis?
7.2 years ago by Amitm ★ 2.1k
1
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0
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2.1k
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Answer: A: RNA Seq coverage
7.2 years ago by Amitm ★ 2.1k
1
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1
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1.6k
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Answer: A: Capillary sequencing data analysis
7.2 years ago by Amitm ★ 2.1k
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2.1k
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Answer: A: Infer loss of heterozygosity from SNP variant frequencies
7.2 years ago by Amitm ★ 2.1k
0
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1
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2.3k
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Answer: A: Assembled TCGA dataset download
7.2 years ago by Amitm ★ 2.1k
1
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0
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1.1k
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Answer: A: how to check which probesets belong to which transcript?
7.2 years ago by Amitm ★ 2.1k
2
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2
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4.5k
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Answer: A: how to understand gene fusion and how to call gene fusion ?
7.2 years ago by Amitm ★ 2.1k
1
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0
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2.0k
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Answer: A: Annotation: From GO to IPS
7.2 years ago by Amitm ★ 2.1k
1
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1
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3.2k
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Answer: A: How to find exact allele frequency for the SNP/indel variants ?
7.3 years ago by Amitm ★ 2.1k
0
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1
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3.2k
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Answer: A: Filtering reads aligned to specific chromosome
7.3 years ago by Amitm ★ 2.1k
0
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0
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2.8k
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Answer: A: TCGA RNAseq normal and tumor samples problem
7.3 years ago by Amitm ★ 2.1k
1
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0
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1.2k
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Answer: A: Interreplicate statistics for microarray data?
7.3 years ago by Amitm ★ 2.1k
4
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0
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7.1k
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Answer: A: Variant caller for low frequency variants
7.3 years ago by Amitm ★ 2.1k
0
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2
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4.6k
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Answer: A: issues with the precalculated lookup in Interproscan-5.17-56.0
7.3 years ago by Amitm ★ 2.1k
2
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1
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5.0k
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Answer: C: Machine Learning - RNAseq
7.3 years ago by Amitm ★ 2.1k
1
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0
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2.2k
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Answer: Answer: Source for Normals for Bladder Cancer RNA-Seq
updated 15 months ago by 39k • written 7.3 years ago by ★ 2.1k
1
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0
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1.6k
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Answer: Answer: Please suggest a suitable tool for GO annotation of a plant de novo assembled tr
updated 11 months ago by 39k • written 7.3 years ago by ★ 2.1k
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1.5k
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Answer: A: mapping known epitopes in a protein sequcence
7.3 years ago by Amitm ★ 2.1k
2
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1
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6.9k
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Answer: Answer: How to calculate enrichment P-value?
updated 10 months ago by 39k • written 7.3 years ago by ★ 2.1k
0
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0
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1.5k
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Answer: Answer: Regarding Human Exon Variant Reference
updated 10 months ago by 39k • written 7.3 years ago by ★ 2.1k
1
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1
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4.0k
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Answer: A: What's wrong with this sample? (kmers found by FastQC of RNA-Seq)
7.4 years ago by Amitm ★ 2.1k
0
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2
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2.8k
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Answer: A: Somatic allele frequency from TCGA in non-coding DNA
7.4 years ago by Amitm ★ 2.1k
3
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2
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2.8k
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Answer: A: Somatic allele frequency from TCGA
7.4 years ago by Amitm ★ 2.1k
17
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1
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23k
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Answer: A: Kmer Content in FastQC failed
7.4 years ago by Amitm ★ 2.1k
1
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0
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3.5k
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Answer: C: microarray meta- analysis
7.4 years ago by Amitm ★ 2.1k
10
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2
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4.8k
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Answer: A: How to decide the quality of RNA-seq analysis
7.4 years ago by Amitm ★ 2.1k
1
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1
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2.1k
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Answer: A: Binning BED file and counting antisense / sense reads
7.4 years ago by Amitm ★ 2.1k
1
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0
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1.5k
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Answer: A: new gene discovery
7.4 years ago by Amitm ★ 2.1k
1
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1
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4.9k
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Answer: A: Somatic mutations from RNA-Seq data of tumor vs. normal
7.4 years ago by Amitm ★ 2.1k
1
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0
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7.4k
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Answer: A: How should I normalized RNA-seq data to draw the gene expression time series cur
8.0 years ago by Amitm ★ 2.1k
2
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0
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39k
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Answer: A: Best Way To Normalize Rna-Seq Data For Expression Profiling
8.0 years ago by Amitm ★ 2.1k
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