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Comment: Comment: How to make the data compatible for DESeq2?
2.7 years ago by Karma ▴ 310
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4.5k
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Comment: C: blast alignemnt query coverage
4.3 years ago by Karma ▴ 310
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4.6k
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Comment: C: Normalization of RNASeq read counts without conditions
4.6 years ago by Karma ▴ 310
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6.5k
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Comment: C: How to rename multiple fastq files
5.2 years ago by Karma ▴ 310
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1
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4.2k
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Comment: A: Where to download Normal exome bam for creating PoN (Panel of Normals) for cance
updated 5.2 years ago by 45k • written 5.2 years ago by ▴ 310
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2.1k
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Comment: C: How to pass arguments in a bash script to perform read alignment to the referenc
5.2 years ago by Karma ▴ 310
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11k
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Comment: A: What Agilent Interval Files (.Bed) Should I Use For Exome Variant Calling With G
5.2 years ago by Karma ▴ 310
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2.1k
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Comment: C: How to pass arguments in a bash script to perform read alignment to the referenc
5.2 years ago by Karma ▴ 310
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2
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2.1k
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Comment: C: How to pass arguments in a bash script to perform read alignment to the referenc
5.2 years ago by Karma ▴ 310
0
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0
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889
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Comment: C: What is configuration required for exome sequence analysis?
5.4 years ago by Karma ▴ 310
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12k
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Comment: C: Converting SNP names from Illumina GSA array to rsID using PLINK
6.6 years ago by Karma ▴ 310
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4.2k
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Comment: Comment: Converting sra to fastq
updated 2.7 years ago by 45k • written 7.5 years ago by ▴ 310
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8.6k
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Comment: C: VCF to ANNOVAR format
7.6 years ago by Karma ▴ 310
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11k
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Comment: C: What Agilent Interval Files (.Bed) Should I Use For Exome Variant Calling With G
7.6 years ago by Karma ▴ 310
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1
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2.4k
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Comment: C: Quantification of a gene that is not in the reference genome
7.6 years ago by Karma ▴ 310
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8.2k
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Comment: C: Is there any way to generate interval list from available exome data?
7.6 years ago by Karma ▴ 310
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14k
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Comment: C: Should I Remove The Unmapped Reads From My Bam ?
7.6 years ago by Karma ▴ 310
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14k
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Comment: A: Should I Remove The Unmapped Reads From My Bam ?
7.6 years ago by Karma ▴ 310
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6.5k
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Comment: C: GATK Workflow for GATK in Cancer Samples
7.6 years ago by Karma ▴ 310
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3.7k
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Comment: C: How to generate FPKM value for each replicates?
7.6 years ago by Karma ▴ 310
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3.7k
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Comment: C: How to generate FPKM value for each replicates?
7.6 years ago by Karma ▴ 310
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1
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4.1k
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Comment: C: RNA-Seq or Exome Seq for Clinical data analysis
7.7 years ago by Karma ▴ 310
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1
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4.5k
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Comment: C: blast alignemnt query coverage
7.7 years ago by Karma ▴ 310
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1
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12k
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Comment: C: Retrieving data from NCBI GEO and RNA-Seq Data Analysis
7.7 years ago by Karma ▴ 310
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1
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2.0k
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Comment: C: What softwares can detect fusion genes from SNP-array data?
7.7 years ago by Karma ▴ 310
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1
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4.5k
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Comment: C: blast alignemnt query coverage
7.7 years ago by Karma ▴ 310
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4.1k
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Comment: C: RNA-Seq or Exome Seq for Clinical data analysis
7.7 years ago by Karma ▴ 310
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0
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4.1k
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Comment: C: RNA-Seq or Exome Seq for Clinical data analysis
7.7 years ago by Karma ▴ 310
1
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0
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4.5k
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Comment: C: blast alignemnt query coverage
7.7 years ago by Karma ▴ 310
0
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0
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4.1k
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Comment: C: RNA-Seq or Exome Seq for Clinical data analysis
7.7 years ago by Karma ▴ 310
2
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1
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4.5k
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Comment: C: blast alignemnt query coverage
7.7 years ago by Karma ▴ 310
1
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1
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4.5k
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Comment: C: blast alignemnt query coverage
7.7 years ago by Karma ▴ 310
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