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Comment: C: GESS exon skipping error
8.3 years ago by WouterDeCoster 48k
1
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7.2k
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Comment: C: Parse fasta header with regex in python
8.3 years ago by WouterDeCoster 48k
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0
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7.2k
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Comment: C: Parse fasta header with regex in python
8.3 years ago by WouterDeCoster 48k
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0
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1.6k
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Comment: C: htseq-count results in missing genes
8.3 years ago by WouterDeCoster 48k
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1
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2.7k
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Comment: C: Deseq2 does not recognize htseq count outputs
8.3 years ago by WouterDeCoster 48k
2
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0
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4.0k
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Comment: C: Is it possible to annotate single genes by snpeff
8.3 years ago by WouterDeCoster 48k
0
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1
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41k
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Comment: C: ggplot2, point with border
8.3 years ago by WouterDeCoster 48k
0
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1
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3.3k
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Comment: C: blast query coverage using perl
8.3 years ago by WouterDeCoster 48k
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0
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1.6k
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Comment: C: how to find position of mi-rna in corresponding EST? i have obtained similarity
8.3 years ago by WouterDeCoster 48k
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0
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2.8k
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Comment: C: RNAseq with quantseq
8.3 years ago by WouterDeCoster 48k
0
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0
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15k
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Comment: C: Multiplex PCR Primer Design Tools
8.3 years ago by WouterDeCoster 48k
0
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1
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2.8k
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Comment: C: RNAseq with quantseq
8.3 years ago by WouterDeCoster 48k
0
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1
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1.6k
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Comment: C: GESS exon skipping error
8.3 years ago by WouterDeCoster 48k
0
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0
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14k
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Comment: C: Retrieving data from NCBI GEO and RNA-Seq Data Analysis
8.3 years ago by WouterDeCoster 48k
0
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1
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2.3k
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Comment: C: What softwares can detect fusion genes from SNP-array data?
8.3 years ago by WouterDeCoster 48k
1
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1
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2.3k
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Comment: C: What softwares can detect fusion genes from SNP-array data?
8.3 years ago by WouterDeCoster 48k
0
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0
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4.8k
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Comment: C: Interproscan GO terms results explanation
8.3 years ago by WouterDeCoster 48k
0
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1
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12k
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Comment: C: Computing TPM from normalized read count from DESEQ
8.3 years ago by WouterDeCoster 48k
0
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1
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12k
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Comment: C: Computing TPM from normalized read count from DESEQ
8.3 years ago by WouterDeCoster 48k
1
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0
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2.7k
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Comment: C: No XIST in Emsembl cdna.fa
8.3 years ago by WouterDeCoster 48k
0
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1
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8.6k
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Comment: C: Interpretation of snpeff results
8.3 years ago by WouterDeCoster 48k
4
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2
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2.7k
views
No XIST in Emsembl cdna.fa
ensembl
updated 8.3 years ago by ★ 1.6k • written 8.3 years ago by 48k
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1.7k
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Comment: C: NGS compute infrastructure
8.3 years ago by WouterDeCoster 48k
1
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0
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7.7k
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Comment: C: HiSeq 4000 PhiX screening and removal using bbduk
8.3 years ago by WouterDeCoster 48k
0
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1
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8.6k
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Comment: C: Interpretation of snpeff results
8.3 years ago by WouterDeCoster 48k
0
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0
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8.6k
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Comment: C: Interpretation of snpeff results
8.3 years ago by WouterDeCoster 48k
3
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1
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4.7k
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Comment: C: RNA-Seq or Exome Seq for Clinical data analysis
8.3 years ago by WouterDeCoster 48k
0
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0
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4.7k
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Comment: C: RNA-Seq or Exome Seq for Clinical data analysis
8.3 years ago by WouterDeCoster 48k
0
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2
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4.7k
views
Comment: C: RNA-Seq or Exome Seq for Clinical data analysis
8.3 years ago by WouterDeCoster 48k
0
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0
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2.0k
views
Comment: C: how to find SNPs in my sequenced reads?
8.3 years ago by WouterDeCoster 48k
0
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0
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4.7k
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Comment: C: RNA-Seq or Exome Seq for Clinical data analysis
8.3 years ago by WouterDeCoster 48k
0
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0
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5.8k
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Comment: C: Working example for VCF visualization in Circos
8.3 years ago by WouterDeCoster 48k
0
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0
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6.4k
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Comment: C: Any implementation of the edgeR in python
8.3 years ago by WouterDeCoster 48k
0
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0
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3.3k
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Comment: C: sequence in different line
8.3 years ago by WouterDeCoster 48k
0
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0
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2.3k
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Comment: C: Targeting causative variant in Exome-Sequence data
8.3 years ago by WouterDeCoster 48k
0
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1
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3.3k
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Comment: C: sequence in different line
8.3 years ago by WouterDeCoster 48k
2
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2
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3.3k
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Comment: C: sequence in different line
8.3 years ago by WouterDeCoster 48k
0
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1
reply
2.3k
views
Comment: C: Targeting causative variant in Exome-Sequence data
8.3 years ago by WouterDeCoster 48k
0
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1
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2.3k
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Comment: C: Targeting causative variant in Exome-Sequence data
8.3 years ago by WouterDeCoster 48k
1
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0
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15k
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Comment: C: Getting error in running GATK (GenomeAnalysisTK-3.7)?
8.3 years ago by WouterDeCoster 48k
0
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0
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3.8k
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Comment: C: readcufflinks shows error in R cummeRbund Package
8.3 years ago by WouterDeCoster 48k
0
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2
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5.1k
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Comment: C: DEseq2 input files
8.3 years ago by WouterDeCoster 48k
2
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0
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2.3k
views
Answer: A: What is the best way to start learning R?
8.3 years ago by WouterDeCoster 48k
0
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1
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2.6k
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Comment: C: R survival analysis SNPs loading data
8.3 years ago by WouterDeCoster 48k
0
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0
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1.5k
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Comment: C: Different reflections from the techincal replicates.
8.3 years ago by WouterDeCoster 48k
0
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0
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3.2k
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Comment: C: Ligand Docking Simulation Programs
8.3 years ago by WouterDeCoster 48k
0
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0
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2.2k
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Comment: C: One of the easy way to achieve read count and RPKM file
8.3 years ago by WouterDeCoster 48k
0
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0
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5.2k
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Comment: C: How to extract all the simple repeats from the hg19 reference genome
8.3 years ago by WouterDeCoster 48k
4
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1
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2.5k
views
Answer: A: Why is there a star in some primer sequences (library preparation)
8.3 years ago by WouterDeCoster 48k
1
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0
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4.3k
views
Answer: A: Soft-clipping of reads in Amplicon-sequenced data
8.3 years ago by WouterDeCoster 48k
7,263 results • Page 69 of 146
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