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Comment: Comment: GEOquery issue
4 weeks ago by Sean Davis 27k
0
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1
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552
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Comment: Comment: GEOquery issue
4 weeks ago by Sean Davis 27k
1
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0
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2.3k
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Comment: Comment: 0 Features for COVID-19 ExpressionSet through GEOQuery
3 months ago by Sean Davis 27k
1
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0
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542
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Comment: Comment: Issue with converting Affy IDs to gene IDs/symbols
4 months ago by Sean Davis 27k
1
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1
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693
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Answer: Answer: GEO Query error
2.4 years ago by Sean Davis 27k
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0
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1.5k
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Comment: Comment: How to analyse GSE Series with Multiple Platforms using R?
2.6 years ago by Sean Davis 27k
1
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1
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1.5k
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Comment: Comment: How to analyse GSE Series with Multiple Platforms using R?
2.6 years ago by Sean Davis 27k
3
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1
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1.5k
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Answer: Answer: How to analyse GSE Series with Multiple Platforms using R?
2.6 years ago by Sean Davis 27k
1
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1
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1.5k
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Comment: Comment: How to analyse GSE Series with Multiple Platforms using R?
2.6 years ago by Sean Davis 27k
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0
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1.3k
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Comment: Comment: filter and annotate vcf file
2.7 years ago by Sean Davis 27k
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0
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738
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Comment: Comment: Customisable DNA Read Simulation for Deleted Reads
2.7 years ago by Sean Davis 27k
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1
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996
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Answer: Answer: Taxonomic identification of NGS reads
2.7 years ago by Sean Davis 27k
2
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1
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1.0k
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Answer: Answer: For GEOquery, do I need to convert my GPL file from .txt to .soft?
2.7 years ago by Sean Davis 27k
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0
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762
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Comment: Comment: Adding repeats in a genome fasta at a particular location without messing up the
3.0 years ago by Sean Davis 27k
3
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1
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1.2k
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Answer: Answer: Hide column label of genes
3.0 years ago by Sean Davis 27k
0
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0
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3.0k
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Comment: Comment: Importing GEO dataset
3.0 years ago by Sean Davis 27k
0
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1
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3.0k
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Comment: Comment: Importing GEO dataset
3.0 years ago by Sean Davis 27k
2
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1
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873
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Answer: Answer: Same MESH ID for two different sub-type
3.0 years ago by Sean Davis 27k
0
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1
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1.4k
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Answer: Answer: Help with accessing GEO dataset
3.0 years ago by Sean Davis 27k
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1
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3.0k
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Comment: Comment: Importing GEO dataset
3.0 years ago by Sean Davis 27k
1
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1
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3.0k
views
Answer: Answer: Importing GEO dataset
3.0 years ago by Sean Davis 27k
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0
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1.1k
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Answer: Answer: Statistical technique for mutation to gene expression link
3.1 years ago by Sean Davis 27k
14
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0
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11k
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Answer: A: Size of BAM file reduces after sorting with samtools
updated 4.0 years ago by 44k • written 9.4 years ago by 27k
1
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0
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1.2k
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Job: Bioconductor and the Channing Division of Network Medicine at Harvard Medical School have created a new project management/software developer/manager…
bioconductor
updated 17 months ago by 44k • written 4.1 years ago by 27k
1
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1
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3.2k
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Answer: A: Question: R programming: group and then compare columns to column and get the mi
updated 4.9 years ago by 44k • written 8.8 years ago by 27k
5
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1
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12k
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Answer: A: Reindex A Vcf File / How To Handle Cosmic Vcf Files
updated 4.9 years ago by 44k • written 11.6 years ago by 27k
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1
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3.5k
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Comment: C: Variant Callers for deep sequencing
updated 4.9 years ago by 44k • written 10.5 years ago by 27k
4
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1
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3.5k
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Answer: A: Variant Callers for deep sequencing
updated 4.9 years ago by 44k • written 10.5 years ago by 27k
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0
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2.6k
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Answer: A: Measuring transcriptional noise
updated 4.9 years ago by 44k • written 8.8 years ago by 27k
0
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1
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2.6k
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Comment: C: Measuring transcriptional noise
updated 4.9 years ago by 44k • written 8.8 years ago by 27k
1
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0
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3.2k
views
Answer: A: calculating target size for a custom panel
updated 4.9 years ago by 44k • written 8.8 years ago by 27k
0
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0
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2.8k
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Comment: C: FASTQ / SAM file processing: combining base QUAL scores
updated 4.9 years ago by 44k • written 8.8 years ago by 27k
1
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0
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2.3k
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Comment: C: How to find the variant type, location and effects (synonymous/nonsynonymous)
updated 4.9 years ago by 44k • written 8.8 years ago by 27k
0
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1
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2.3k
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Comment: C: How to find the variant type, location and effects (synonymous/nonsynonymous)
updated 4.9 years ago by 44k • written 8.8 years ago by 27k
4
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1
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3.7k
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Answer: A: Ensembl BioMart - How to get Transcript IDs version increment?
updated 4.9 years ago by 44k • written 8.8 years ago by 27k
0
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0
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1.7k
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Answer: A: feature selection for specific disease groups
updated 4.9 years ago by 44k • written 8.8 years ago by 27k
0
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0
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6.8k
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Answer: A: Multiprocessing in Python with subprocess to align several files with coding DNA
updated 4.9 years ago by 44k • written 8.8 years ago by 27k
0
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1
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1.7k
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Comment: C: feature selection for specific disease groups
updated 4.9 years ago by 44k • written 8.8 years ago by 27k
0
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0
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3.2k
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Comment: Comment: analyzing RNAseq data in cytoscape
updated 4.9 years ago by 44k • written 8.8 years ago by 27k
0
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0
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5.8k
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Comment: C: machine learning datasets for bioinformatics
updated 4.9 years ago by 44k • written 8.8 years ago by 27k
0
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1
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5.7k
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Comment: C: DNA microarray data available from TCGA?
updated 4.9 years ago by 44k • written 8.8 years ago by 27k
1
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0
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3.0k
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Comment: C: Request for karyotypically sorted Ensembl reference fasta and its dbSNP vcf for
updated 4.9 years ago by 44k • written 8.8 years ago by 27k
1
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1
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3.0k
views
Comment: C: Request for karyotypically sorted Ensembl reference fasta and its dbSNP vcf for
updated 4.9 years ago by 44k • written 8.8 years ago by 27k
0
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0
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6.8k
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Comment: C: Combining Two Platforms Affy Hgu133A And Hgu133B
updated 4.9 years ago by 44k • written 12.0 years ago by 27k
1
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0
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2.2k
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Comment: C: Expression of target genes using SRA Dataset
updated 4.9 years ago by 44k • written 8.8 years ago by 27k
0
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0
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3.2k
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Answer: A: 95%CI for Rsquared in linear regression
updated 4.9 years ago by 44k • written 8.8 years ago by 27k
2
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0
replies
4.8k
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Comment: C: HiSeq vs GA for RNASeqV2 on TCGA
updated 4.9 years ago by 44k • written 8.8 years ago by 27k
1
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0
replies
3.2k
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Comment: C: Mixed opinions on somatic variant calling method
updated 4.9 years ago by 44k • written 8.8 years ago by 27k
2
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1
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3.2k
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Comment: C: Mixed opinions on somatic variant calling method
updated 4.9 years ago by 44k • written 8.8 years ago by 27k
2
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0
replies
4.9k
views
Comment: C: How to create color range for RPKM/FPKM using R?
updated 4.9 years ago by 44k • written 10.5 years ago by 27k
1,985 results • Page 1 of 40
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