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2
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Comment: C: IGV white read color meaning
8.8 years ago by WouterDeCoster 48k
0
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2.3k
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Comment: C: PCA of Cuffdiff output
8.8 years ago by WouterDeCoster 48k
0
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0
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16k
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Comment: C: GC Content of Fasta file --- Python Help
8.8 years ago by WouterDeCoster 48k
0
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0
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2.5k
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Comment: C: error in bowtie 2
8.8 years ago by WouterDeCoster 48k
0
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1
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2.1k
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Comment: C: extracting targe genes of a list of TFs
8.8 years ago by WouterDeCoster 48k
2
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1
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2.7k
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Answer: A: In GATK, SNPs and INDELs are called separately or together?
8.8 years ago by WouterDeCoster 48k
0
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1
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16k
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Comment: C: GC Content of Fasta file --- Python Help
8.8 years ago by WouterDeCoster 48k
0
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0
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1.3k
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Comment: C: Data Set Needed: Genetic Association Analysis or Gene Set Enrichment Analysis
8.8 years ago by WouterDeCoster 48k
0
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0
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2.5k
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Comment: C: error in bowtie 2
8.8 years ago by WouterDeCoster 48k
0
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0
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5.1k
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Comment: C: Next-Gen Sequencing Tutorials On Cubelp (Cranfield Bioinformatics Electronic Lea
8.8 years ago by WouterDeCoster 48k
0
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0
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3.5k
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Comment: C: How do you find ballgown package for differential expression analysis?
8.8 years ago by WouterDeCoster 48k
0
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1
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2.1k
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Comment: C: strand-biased mutation analysis on WES data
8.8 years ago by WouterDeCoster 48k
0
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0
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3.2k
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Answer: A: Why some questions in OPEN section of the Biostars.org have "(Closed)" at the be
8.8 years ago by WouterDeCoster 48k
0
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0
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5.0k
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Comment: C: What is the fastest way to add 'Ns' to variable length sequences in a .fasta suc
8.8 years ago by WouterDeCoster 48k
0
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0
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3.8k
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Comment: C: Can I merge fastq files of a same sample from two sequencers for gene expression
8.8 years ago by WouterDeCoster 48k
2
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0
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4.6k
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Answer: A: How to merge paired-end reads from sam files?
8.8 years ago by WouterDeCoster 48k
0
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1
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5.0k
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Comment: C: What is the fastest way to add 'Ns' to variable length sequences in a .fasta suc
8.8 years ago by WouterDeCoster 48k
1
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1
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5.0k
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Comment: C: What is the fastest way to add 'Ns' to variable length sequences in a .fasta suc
8.8 years ago by WouterDeCoster 48k
1
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1
reply
4.6k
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Comment: C: How to merge paired-end reads from sam files?
8.8 years ago by WouterDeCoster 48k
2
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1
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4.6k
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Answer: A: How to merge paired-end
8.8 years ago by WouterDeCoster 48k
0
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0
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13k
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Comment: C: BAM to BIGWIG
8.8 years ago by WouterDeCoster 48k
1
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0
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27k
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Comment: C: finding adapters from fastq file
8.8 years ago by WouterDeCoster 48k
1
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0
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2.2k
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Comment: C: What You Call "Coding Region" On Ensembl Variation
8.8 years ago by WouterDeCoster 48k
1
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1
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9.0k
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Answer: A: How to prepare .gct file for GSEA software?
8.8 years ago by WouterDeCoster 48k
1
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0
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27k
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Comment: C: finding adapters from fastq file
8.8 years ago by WouterDeCoster 48k
3
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3
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27k
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Comment: C: finding adapters from fastq file
8.8 years ago by WouterDeCoster 48k
1
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0
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3.4k
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Comment: C: How to differentiate SNPs Vs Sequencing error in RNA Seq?
8.8 years ago by WouterDeCoster 48k
0
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0
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2.6k
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Comment: C: Is there an C++ tool to implement GATK ?
8.8 years ago by WouterDeCoster 48k
0
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2
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2.6k
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Comment: C: Is there an C++ tool to implement GATK ?
8.8 years ago by WouterDeCoster 48k
0
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0
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5.1k
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Comment: C: gene ontology visualisation
8.8 years ago by WouterDeCoster 48k
0
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1
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2.8k
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Answer: A: problem in running vcf-consensus command
8.8 years ago by WouterDeCoster 48k
0
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0
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3.1k
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Comment: C: How to compare two groups of 3 samples
8.8 years ago by WouterDeCoster 48k
1
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0
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6.5k
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Answer: A: DESeq2 input for DE analysis
8.8 years ago by WouterDeCoster 48k
1
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1
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3.3k
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Comment: C: Optimal number of samples needed to detect a variant from panel sequencing
8.8 years ago by WouterDeCoster 48k
1
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0
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4.3k
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Comment: C: how to import agilent data in r
8.8 years ago by WouterDeCoster 48k
0
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0
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7.0k
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Comment: C: vcf-consensus outputs sequence same as reference
8.8 years ago by WouterDeCoster 48k
1
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1
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12k
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Comment: C: heatmap using FPKM values
8.8 years ago by WouterDeCoster 48k
1
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1
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12k
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Comment: C: heatmap using FPKM values
8.8 years ago by WouterDeCoster 48k
0
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0
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1.7k
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Comment: C: Anti-oligonucleotide design for blocking microRNA, is it even possible?
8.8 years ago by WouterDeCoster 48k
0
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1
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1.7k
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Comment: C: Anti-oligonucleotide design for blocking microRNA, is it even possible?
8.8 years ago by WouterDeCoster 48k
1
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0
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4.7k
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Comment: C: Number of homozygous and heterozygous variants
8.8 years ago by WouterDeCoster 48k
0
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0
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19k
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Comment: C: Calculating FPKM after htseq-count
8.8 years ago by WouterDeCoster 48k
1
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0
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2.0k
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Comment: C: Free online Ensembl course
8.8 years ago by WouterDeCoster 48k
0
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1
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19k
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Comment: C: Calculating FPKM after htseq-count
8.8 years ago by WouterDeCoster 48k
0
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0
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2.9k
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Comment: C: Identification of SNP effect on amino acid. Issue with SnpEff
8.8 years ago by WouterDeCoster 48k
2
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0
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5.9k
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Comment: C: Variant Call Format (VCF)
8.8 years ago by WouterDeCoster 48k
1
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1
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2.9k
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Comment: C: Identification of SNP effect on amino acid. Issue with SnpEff
8.8 years ago by WouterDeCoster 48k
0
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1
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5.9k
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Comment: C: Variant Call Format (VCF)
8.8 years ago by WouterDeCoster 48k
1
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1
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4.7k
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Comment: C: Number of homozygous and heterozygous variants
8.8 years ago by WouterDeCoster 48k
1
vote
1
reply
4.7k
views
Answer: A: Number of homozygous and heterozygous variants
8.8 years ago by WouterDeCoster 48k
7,263 results • Page 95 of 146
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