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Comment: C: Why there are genes that are not present in TCGA normalized rna-seq data?
9.6 years ago by WouterDeCoster 48k
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3.8k
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Comment: C: Very basic for a student: How to analyse RPKM expression data to identify genes
9.6 years ago by WouterDeCoster 48k
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6.9k
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Answer: A: SNP coordinate systems in UCSC LiftOver (hg19), NCBI Remap (GRCh37(hg19)) and db
9.6 years ago by WouterDeCoster 48k
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4.5k
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Answer: A: NGS analysis on windows
9.6 years ago by WouterDeCoster 48k
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Comment: C: What to do with disease-associated SNPs laying intergenic regions?
9.6 years ago by WouterDeCoster 48k
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12k
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Answer: A: [Python] How to convert a list to a dictionary if dict() does not work without u
9.6 years ago by WouterDeCoster 48k
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1
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2.2k
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Answer: A: What to do with disease-associated SNPs laying intergenic regions?
9.6 years ago by WouterDeCoster 48k
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2.2k
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Comment: C: Error in Commands
9.6 years ago by WouterDeCoster 48k
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5.4k
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Comment: C: WGCNA module significance ?
9.6 years ago by WouterDeCoster 48k
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1.8k
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Comment: C: alternation for Integrated Pathway Analysis Database for Systematic Enrichment A
9.6 years ago by WouterDeCoster 48k
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3.0k
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Answer: A: RNA Seq coverage
9.6 years ago by WouterDeCoster 48k
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1.8k
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Comment: C: Which population should be chosen?
9.6 years ago by WouterDeCoster 48k
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1.8k
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Comment: C: Which population should be chosen?
9.6 years ago by WouterDeCoster 48k
2
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1
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13k
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Answer: A: Kallisto New RNA-seq quantification method discussion
9.6 years ago by WouterDeCoster 48k
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5.1k
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Comment: C: Inconsistencies between RNA Seq and PCR
9.6 years ago by WouterDeCoster 48k
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3.2k
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Comment: C: Convert genotype to nucleotide genotype?
9.6 years ago by WouterDeCoster 48k
1
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1
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18k
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Comment: C: Combine lines into one line after specific line identifier
9.6 years ago by WouterDeCoster 48k
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2
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2.0k
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Comment: C: More than one possible mapping place for a read
9.6 years ago by WouterDeCoster 48k
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0
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3.5k
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Answer: A: UMI for Exome Target Sequencing
9.6 years ago by WouterDeCoster 48k
0
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1
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5.1k
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Answer: A: Inconsistencies between RNA Seq and PCR
9.6 years ago by WouterDeCoster 48k
4
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0
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4.2k
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Answer: A: What's the difference between Bioconductor's knownGene and ensGene annotation pa
9.6 years ago by WouterDeCoster 48k
0
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1
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3.2k
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Comment: C: Convert genotype to nucleotide genotype?
9.6 years ago by WouterDeCoster 48k
0
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1
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3.2k
views
Answer: A: Convert genotype to nucleotide genotype?
9.6 years ago by WouterDeCoster 48k
1
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1
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3.2k
views
Comment: C: Convert genotype to nucleotide genotype?
9.6 years ago by WouterDeCoster 48k
1
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0
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4.0k
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Comment: C: Adding headers/ identifiers to List of lists in R
9.6 years ago by WouterDeCoster 48k
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2
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2.0k
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Answer: A: More than one possible mapping place for a read
9.6 years ago by WouterDeCoster 48k
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3.3k
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Comment: C: reading microarray data in R
9.6 years ago by WouterDeCoster 48k
2
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1.7k
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Comment: C: REMOVAL OF GI NUMBERS FROM MSA FILE
9.6 years ago by WouterDeCoster 48k
1
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1
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8.6k
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Comment: C: GO term enrichment analysis using DAVID: How to start data analysis?
9.6 years ago by WouterDeCoster 48k
1
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0
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3.3k
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Answer: A: reading microarray data in R
9.6 years ago by WouterDeCoster 48k
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1
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3.9k
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Answer: A: How to estimate the power of association test for small sample size
9.6 years ago by WouterDeCoster 48k
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1
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2.6k
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Comment: C: How do I replace a value used in script with a range of values in a file?
9.6 years ago by WouterDeCoster 48k
1
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1
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7.8k
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Comment: C: PCA on VCF
9.6 years ago by WouterDeCoster 48k
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0
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2.6k
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Answer: C: Problem to install the package BCBio from biopython - not available?
9.6 years ago by WouterDeCoster 48k
1
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1
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2.7k
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Comment: C: HTSeq-count output files sizes are always 10mb
9.6 years ago by WouterDeCoster 48k
1
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0
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26k
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Answer: A: How to define the gene length for RPKM calculation
9.6 years ago by WouterDeCoster 48k
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0
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18k
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Comment: C: Combine lines into one line after specific line identifier
9.6 years ago by WouterDeCoster 48k
1
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0
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3.3k
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Comment: C: TCGA Analysis - Generating Count files using htseq
9.6 years ago by WouterDeCoster 48k
1
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0
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7.9k
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Comment: C: rename reads in fastq files
updated 9.6 years ago by 45k • written 9.7 years ago by 48k
0
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0
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1.7k
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Answer: A: Proper reference set selection in enrichment analysis
9.7 years ago by WouterDeCoster 48k
1
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1
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13k
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Comment: C: FASTA file of fixed length
9.7 years ago by WouterDeCoster 48k
2
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1
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13k
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Comment: C: FASTA file of fixed length
9.7 years ago by WouterDeCoster 48k
1
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0
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3.6k
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Comment: C: hg18 vs hg19 in SNP6.0 data
9.7 years ago by WouterDeCoster 48k
0
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0
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2.0k
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Comment: C: Pathway analysis of miRNA?
9.7 years ago by WouterDeCoster 48k
3
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2.9k
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Answer: A: What are the best tools for mapping RNASeq paired-end data (HiSeq2000) for funga
9.7 years ago by WouterDeCoster 48k
0
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1
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3.6k
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Answer: A: hg18 vs hg19 in SNP6.0 data
9.7 years ago by WouterDeCoster 48k
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0
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3.3k
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Comment: C: Gene level RNA seq expression measure
9.7 years ago by WouterDeCoster 48k
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0
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2.6k
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Answer: A: Python or shell scripting code ro count individual mapped reads of amplicons
9.7 years ago by WouterDeCoster 48k
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0
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5.5k
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Comment: C: How to do gene enrichment analysis?
9.7 years ago by WouterDeCoster 48k
0
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0
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3.6k
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Comment: C: biopython script to preprocess raw RNA-seq reads (quality filtering, polyA and a
9.7 years ago by WouterDeCoster 48k
7,263 results • Page 144 of 146
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