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Answer: A: How different the different ChIP-seq samples are ....
updated 3.7 years ago by 40k • written 9.3 years ago by ★ 4.2k
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Answer: A: Test for recombination in a clonal tetraploid?
updated 3.7 years ago by 40k • written 9.3 years ago by ★ 4.2k
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Answer: A: The interface between bioinformatics and biophysics (with the possibility of bio
updated 3.8 years ago by 40k • written 9.4 years ago by ★ 4.2k
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3.7k
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Answer: A: Data Management System For Bioinformatics?
updated 3.8 years ago by 40k • written 9.7 years ago by ★ 4.2k
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Answer: A: NOT RESETTING NORMAL error using Varscan2
updated 4.0 years ago by 40k • written 8.8 years ago by ★ 4.2k
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Answer: A: Genomecoveragebed - Bedtool For Reporting Per Base Genome Coverage
updated 4.0 years ago by 40k • written 11.6 years ago by ★ 4.2k
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Answer: A: Online Bioinformatics Training Options
updated 4.0 years ago by 40k • written 11.6 years ago by ★ 4.2k
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Answer: A: Looking For Chip-Seq Data Oct4/Sox2/Nanog 36Bp Or More
updated 4.0 years ago by 40k • written 11.9 years ago by ★ 4.2k
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Answer: A: How Do You Manage Your Files & Directories For Your Projects ?
updated 4.0 years ago by 40k • written 12.3 years ago by ★ 4.2k
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Answer: A: The Longest Chromosome > Sizeof(Int32)
updated 4.7 years ago by 40k • written 12.0 years ago by ★ 4.2k
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Answer: A: Replicates In Chip-Seq
updated 4.7 years ago by 40k • written 10.1 years ago by ★ 4.2k
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Answer: A: What is differences and similarites between NCI60, CCLE, CMAP?
7.1 years ago by Ying W ★ 4.2k
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Answer: A: step by step mass spectrometry proteomics
7.9 years ago by Ying W ★ 4.2k
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4.3k
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Answer: A: Alternative for BGI WEGO
7.9 years ago by Ying W ★ 4.2k
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Answer: A: pipeline of analyses to identify functional loops of chromosomes
7.9 years ago by Ying W ★ 4.2k
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Answer: A: ENCODE DNase Hypersensitivity narrowPeak scores
7.9 years ago by Ying W ★ 4.2k
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Answer: Answer: rsubread: featureCounts, extending ChIP-seq reads, counting the fragments
updated 12 months ago by 40k • written 8.1 years ago by ★ 4.2k
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Answer: Answer: Is strand important when it comes to DNAse and ChIP-Seq peak calling?
updated 12 months ago by 40k • written 8.1 years ago by ★ 4.2k
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Answer: Answer: TCGA: How to tell if the data is exome or WGS?
updated 12 months ago by 40k • written 8.1 years ago by ★ 4.2k
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Answer: Answer: R: bisulfite squencing PCR plot
updated 11 months ago by 40k • written 8.1 years ago by ★ 4.2k
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2
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Answer: Answer: Correcting batch effects between RPKM datasets?
updated 11 months ago by 40k • written 8.2 years ago by ★ 4.2k
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Answer: A: illumina beadarray expresion matrix transformation problem
8.2 years ago by Ying W ★ 4.2k
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Answer: A: Profiling / benchmarking bioinformatics tools
8.2 years ago by Ying W ★ 4.2k
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Answer: Answer: EDASeq - Problem "longer object length is not a multiple of shorter object lengt
updated 11 months ago by 40k • written 8.2 years ago by ★ 4.2k
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16k
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Answer: Answer: Limma package: explanation makeContrasts examples
updated 11 months ago by 40k • written 8.2 years ago by ★ 4.2k
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1
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4.0k
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Answer: A: Normalization of DNase-seq samples with globally different chromatin structures
8.2 years ago by Ying W ★ 4.2k
4
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1
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25k
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Answer: A: Run multiple fastq.gz files with FastQC and yield single report?
8.2 years ago by Ying W ★ 4.2k
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1.6k
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Answer: A: Can we call a protein under undergone ChIP as ChIP'd protein? Is it formal?
8.2 years ago by Ying W ★ 4.2k
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Answer: Answer: QC of ChIPseq data (controlling false negatives)
updated 10 months ago by 40k • written 8.2 years ago by ★ 4.2k
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2.7k
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Answer: A: Is there any differnce between using biomaRt package under R to retrieve gene in
8.3 years ago by Ying W ★ 4.2k
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1
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2.4k
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Answer: A: Strucutral Variant analysis in WES
8.3 years ago by Ying W ★ 4.2k
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2.7k
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Answer: A: Problems in plotting phylogenetic tree and principal component analysis
8.3 years ago by Ying W ★ 4.2k
1
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1
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2.9k
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Answer: Answer: How to produce a hom/het snp frequency table
updated 9 months ago by 40k • written 8.3 years ago by ★ 4.2k
7
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1
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4.5k
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Answer: A: Sliding Window for CNV Analysis
8.3 years ago by Ying W ★ 4.2k
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0
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2.0k
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Answer: A: tabix query retruns multiple variants for a single position. Is it expected?
8.3 years ago by Ying W ★ 4.2k
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2
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6.0k
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Answer: Answer: How to handle chr Y data in BAM files from exome sequencing of human females
updated 9 months ago by 40k • written 8.3 years ago by ★ 4.2k
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1
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1.8k
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Answer: A: Regarding deleted SNPs (in dbSNP) due to mapping or clustering errors found in V
8.3 years ago by Ying W ★ 4.2k
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1
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2.5k
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Answer: A: What does this mean in my read (samtools)
8.3 years ago by Ying W ★ 4.2k
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1
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3.0k
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Answer: Answer: Named variants to Rsids or coordinates or Haplotype?
updated 9 months ago by 40k • written 8.3 years ago by ★ 4.2k
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Answer: A: What is the difference between fine-mapping and targeted sequencing?
8.3 years ago by Ying W ★ 4.2k
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Answer: A: Locate A SNP Number of Reads for Variance and References using Pysam
8.3 years ago by Ying W ★ 4.2k
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5.6k
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Answer: Answer: gVCF from VCF and BAM
updated 9 months ago by 40k • written 8.3 years ago by ★ 4.2k
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1
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2.5k
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Answer: Answer: Quality scores in ICGC simple somatic mutation file
updated 9 months ago by 40k • written 8.3 years ago by ★ 4.2k
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0
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Answer: A: ICGC/TCGA clinical data. Specimen_interval longer than donor survival time?
8.3 years ago by Ying W ★ 4.2k
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1
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8.2k
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Answer: Answer: Samtools mpileup quality scores all zero
updated 9 months ago by 40k • written 8.3 years ago by ★ 4.2k
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1
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1.6k
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Answer: A: mitochondrial variants in familial disease
8.3 years ago by Ying W ★ 4.2k
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1
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3.5k
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Answer: A: Comparing TMM and RSEM RNASeq data
8.3 years ago by Ying W ★ 4.2k
2
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0
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4.8k
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Answer: A: insert figure and code in the post of Biostars?
8.3 years ago by Ying W ★ 4.2k
1
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1
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4.5k
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Answer: A: sam/bam file handling -> new tools?
8.5 years ago by Ying W ★ 4.2k
1
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1
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3.6k
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Answer: A: Illumina BeadChip Replicate Probes
8.5 years ago by Ying W ★ 4.2k
126 results • Page 1 of 3
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