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News: Biocuration 2016 review
opendata ontology conference biocuration
updated 2.6 years ago by 45k • written 9.6 years ago by 27k
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News: Call for papers for Rpackage and Bioconductor channels on F1000Research
bioconductor R
updated 2.6 years ago by 45k • written 9.6 years ago by 27k
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Comment: C: The NIH Software Discovery Index | We invite your comments
9.6 years ago by Sean Davis 27k
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5.0k
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Comment: C: problem loading library in R
9.6 years ago by Sean Davis 27k
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Comment: C: Which Bioinformatic Friendly Pipeline Building Framework?
9.7 years ago by Sean Davis 27k
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Comment: C: Separating gene list into chromatin domains and analysing separately within each
9.7 years ago by Sean Davis 27k
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Job: Staff Scientist, Laboratory of Genome Integrity, NCI, NIH
NIH staff-scientist
updated 2.6 years ago by 45k • written 9.7 years ago by 27k
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3.2k
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Comment: C: Separating gene list into chromatin domains
9.7 years ago by Sean Davis 27k
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5.7k
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Clients to access TCGA data from R and Python
tcga r
9.7 years ago by Sean Davis 27k
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Comment: C: 80% of FPKM values are zero after cufflinks
9.7 years ago by Sean Davis 27k
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Comment: C: Bioconductor as a source for the dependencies of an R package?
9.7 years ago by Sean Davis 27k
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Answer: A: Find occurrence of short pattern in fasta with several sequences and ouput it to
9.7 years ago by Sean Davis 27k
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5.0k
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Comment: Comment: How to annotate positions using biomaRt R package?
updated 3.4 years ago by 45k • written 9.7 years ago by 27k
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2.1k
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Approaches in a post-WGS era for encoding genome information
genome
updated 3.9 years ago by 45k • written 11.2 years ago by 27k
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2.3k
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Comment: Comment: expression matrix from two dyes array
updated 3.4 years ago by 45k • written 9.7 years ago by 27k
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2.3k
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Answer: Answer: expression matrix from two dyes array
updated 3.4 years ago by 45k • written 9.7 years ago by 27k
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2.4k
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Comment: Comment: DNAcopy package use to find the copy number
updated 3.4 years ago by 45k • written 9.8 years ago by 27k
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1.4k
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Comment: Comment: Sequence analysis of Unknown genes from datasets
updated 3.4 years ago by 45k • written 9.8 years ago by 27k
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3.8k
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Answer: Answer: FASTQ / SAM file processing: combining base QUAL scores
updated 3.4 years ago by 45k • written 9.8 years ago by 27k
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4.1k
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Comment: Comment: What does it mean for a snp to be enriched?
updated 3.4 years ago by 45k • written 9.8 years ago by 27k
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4.9k
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Comment: Comment: limma: blocking for batch/individual in paired samples with multiple tissues
updated 3.4 years ago by 45k • written 9.8 years ago by 27k
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4.1k
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Comment: Comment: What does it mean for a snp to be enriched?
updated 3.4 years ago by 45k • written 9.8 years ago by 27k
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Comment: Comment: vcf-merge gives empty output or run forever
updated 3.3 years ago by 45k • written 9.8 years ago by 27k
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Answer: Answer: read FASTA file in R, including description information
updated 3.6 years ago by 45k • written 9.8 years ago by 27k
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2.7k
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Comment: Comment: List of SNP's for alleles at a particular locus
updated 3.3 years ago by 45k • written 9.8 years ago by 27k
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Answer: Answer: Selectively downloading sequences from miRBase
updated 3.3 years ago by 45k • written 9.8 years ago by 27k
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2.7k
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Comment: C: List of SNP's for alleles at a particular locus
9.8 years ago by Sean Davis 27k
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2.8k
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Comment: Comment: NGS hybrid reads
updated 3.3 years ago by 45k • written 9.8 years ago by 27k
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Answer: Answer: Trueseq Vs Nextera
updated 3.3 years ago by 45k • written 9.8 years ago by 27k
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2.8k
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Comment: Comment: NGS hybrid reads
updated 3.3 years ago by 45k • written 9.8 years ago by 27k
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Answer: Answer: Get miRNA expression from RNA-seq
updated 3.3 years ago by 45k • written 9.8 years ago by 27k
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2.8k
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Answer: Answer: NGS hybrid reads
updated 3.3 years ago by 45k • written 9.8 years ago by 27k
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Answer: A: Differential binding analysis of motif-containing peaks
9.8 years ago by Sean Davis 27k
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Answer: A: How to get the coverage of whole gene in exome sequencing data
9.8 years ago by Sean Davis 27k
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Comment: C: BWA missing reads in output
9.8 years ago by Sean Davis 27k
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Answer: A: How to find the variant type, location and effects (synonymous/nonsynonymous)
9.8 years ago by Sean Davis 27k
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Comment: C: Ensembl BioMart - How to get Transcript IDs version increment?
9.8 years ago by Sean Davis 27k
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Comment: C: Multiprocessing in Python with subprocess to align several files with coding DNA
9.8 years ago by Sean Davis 27k
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Answer: A: machine learning datasets for bioinformatics
9.8 years ago by Sean Davis 27k
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6.6k
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Comment: C: DNA microarray data available from TCGA?
9.8 years ago by Sean Davis 27k
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7.9k
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Answer: A: Differential expression gene list from TCGA level 3 RNASeq V2 datasets downloade
9.8 years ago by Sean Davis 27k
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Comment: C: Workflow management software for pipeline development in NGS
9.8 years ago by Sean Davis 27k
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Answer: A: filtering only differentially expressed genes
9.8 years ago by Sean Davis 27k
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3.4k
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Comment: C: Recalculate QUAL and INFO fields for a subset of samples in a VCF
9.8 years ago by Sean Davis 27k
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1
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3.9k
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Answer: A: structure of SOFT files
9.8 years ago by Sean Davis 27k
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Answer: A: methods for having accurate Microarray Data
9.8 years ago by Sean Davis 27k
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Comment: C: gap filling solution
9.8 years ago by Sean Davis 27k
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Comment: C: what information can I obtain from a bunch of proteins IDs?
9.8 years ago by Sean Davis 27k
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Comment: C: Make bam index human readable
9.9 years ago by Sean Davis 27k
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Comment: C: ncbi gds datasets
9.9 years ago by Sean Davis 27k
1,985 results • Page 9 of 40
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