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Answer:
Answer: Filtering methods for samtools or GATK
2.6 years ago by
LChart
5.1k
0
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1
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3.8k
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Comment:
Comment: BULK mRNA-seq with UMIs. Do I need to normalize by gene length?
2.6 years ago by
LChart
5.1k
0
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2
replies
2.6k
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Comment:
Comment: Downloading NT chunks from NCBI and creating a BLAST database
2.6 years ago by
LChart
5.1k
1
vote
0
replies
1.4k
views
Comment:
Comment: Sample size, GxE GWAS
2.7 years ago by
LChart
5.1k
2
votes
1
reply
1.3k
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Answer:
Answer: Is there a way to download the KEGG output (gene - KO) directly?
2.7 years ago by
LChart
5.1k
0
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1
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1.3k
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Answer:
Answer: gwas summary statistics
2.7 years ago by
LChart
5.1k
3
votes
0
replies
928
views
Answer:
Answer: TPM or TMM for gene expression correlation and distribution
2.7 years ago by
LChart
5.1k
2
votes
0
replies
1.7k
views
Comment:
Comment: GWAS: population covariates - should the x-chromosome in addition to autosomes?
2.7 years ago by
LChart
5.1k
3
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1
reply
1.7k
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Answer:
Answer: GWAS: population covariates - should the x-chromosome in addition to autosomes?
2.7 years ago by
LChart
5.1k
1
vote
1
reply
989
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Comment:
Comment: Is there any recommended RNAseq ranking for DEGs/driver genes
2.7 years ago by
LChart
5.1k
0
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0
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1.9k
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Comment:
Comment: WGCNA: problem with how to avoid huge modules
2.7 years ago by
LChart
5.1k
1
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0
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1.4k
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Comment:
Comment: In GWAS what is the point of regressing a quantitative phenotype on covariates f
2.7 years ago by
LChart
5.1k
0
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2
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1.9k
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Comment:
Comment: WGCNA: problem with how to avoid huge modules
2.7 years ago by
LChart
5.1k
1
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0
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2.7k
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Comment:
Comment: UMAP Cluster separation
2.7 years ago by
LChart
5.1k
0
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1
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2.7k
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Comment:
Comment: UMAP Cluster separation
2.7 years ago by
LChart
5.1k
1
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1
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1.9k
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Comment:
Comment: WGCNA: problem with how to avoid huge modules
2.7 years ago by
LChart
5.1k
1
vote
1
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2.6k
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Answer:
Answer: Why is the fraction of mRNA transcripts captured per cell so low?
2.7 years ago by
LChart
5.1k
2
votes
1
reply
1.7k
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Comment:
Comment: HaplotypeCaller: GVCF-Mode or VCF for variant calling of single sample?
2.7 years ago by
LChart
5.1k
0
votes
0
replies
1.0k
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Comment:
Comment: Is the RNA- sequencing quality too bad for analysis?
2.7 years ago by
LChart
5.1k
0
votes
0
replies
1.3k
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Comment:
Comment: The Biostar Herald for Tuesday, December 27, 2022
2.7 years ago by
LChart
5.1k
2
votes
1
reply
1.8k
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Comment:
Comment: Mutect2 read orientation bias filter effect on Somatic variant calling
2.7 years ago by
LChart
5.1k
1
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0
replies
3.0k
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Comment:
Comment: Interesting discrepancy between NGS (Illumina) and Sanger seq.
2.7 years ago by
LChart
5.1k
1
vote
2
replies
3.0k
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Comment:
Comment: Interesting discrepancy between NGS (Illumina) and Sanger seq.
2.7 years ago by
LChart
5.1k
0
votes
1
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1.5k
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Comment:
Comment: Redirect Stdout From twoBitToFa in Bash
2.7 years ago by
LChart
5.1k
1
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0
replies
1.1k
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Comment:
Comment: scRNA seq with seurat: how do I add a column to the metadata?
2.8 years ago by
LChart
5.1k
1
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0
replies
956
views
Answer:
Answer: Can variant exist in VCF even if no samples have that variant
2.8 years ago by
LChart
5.1k
2
votes
1
reply
1.8k
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Answer:
Answer: How to make scanpy read gene names to plot instead of read sequences
2.8 years ago by
LChart
5.1k
0
votes
1
reply
1.1k
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Comment:
Comment: Why can't I quantify the peaks (scATAC)?
2.8 years ago by
LChart
5.1k
0
votes
1
reply
1.8k
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Comment:
Comment: add 1/2 to fastq header
2.8 years ago by
LChart
5.1k
1
vote
1
reply
954
views
Comment:
Comment: Genotyping
2.8 years ago by
LChart
5.1k
1
vote
0
replies
1.8k
views
Comment:
Comment: add 1/2 to fastq header
2.8 years ago by
LChart
5.1k
0
votes
0
replies
1.1k
views
Comment:
Comment: Problem in annotation function for visualization of points in PCA plot
2.8 years ago by
LChart
5.1k
0
votes
0
replies
3.8k
views
Comment:
Comment: Automated way to pull representative/RefSeq genome using full species name?
2.8 years ago by
LChart
5.1k
0
votes
1
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1.2k
views
Comment:
Comment: SNPs in LD with fine-mapped SNPs, are they equally likely to be causative?
2.8 years ago by
LChart
5.1k
0
votes
1
reply
3.8k
views
Comment:
Comment: Automated way to pull representative/RefSeq genome using full species name?
2.8 years ago by
LChart
5.1k
0
votes
0
replies
1.1k
views
Comment:
Comment: How to create in silico circulating tumour DNA samples for analysis benchmarking
2.8 years ago by
LChart
5.1k
0
votes
1
reply
1.2k
views
Comment:
Comment: SNPs in LD with fine-mapped SNPs, are they equally likely to be causative?
2.8 years ago by
LChart
5.1k
2
votes
1
reply
1.1k
views
Answer:
Answer: How to create in silico circulating tumour DNA samples for analysis benchmarking
2.8 years ago by
LChart
5.1k
1
vote
0
replies
4.0k
views
Comment:
Comment: BioStars and ChatGPT
2.8 years ago by
LChart
5.1k
1
vote
0
replies
1.4k
views
Answer:
Answer: How to run UMAP on single cell results from 2 different runs?
2.8 years ago by
LChart
5.1k
0
votes
1
reply
4.0k
views
Comment:
Comment: BioStars and ChatGPT
2.8 years ago by
LChart
5.1k
3
votes
3
replies
4.0k
views
Comment:
Comment: BioStars and ChatGPT
2.8 years ago by
LChart
5.1k
0
votes
0
replies
4.0k
views
Answer:
Answer: Database for taxonomic assignment of shotgun sequencing reads data
2.8 years ago by
LChart
5.1k
0
votes
1
reply
2.1k
views
Comment:
Comment: Box plots with logFC values
2.8 years ago by
LChart
5.1k
1
vote
1
reply
3.8k
views
Comment:
Comment: Automated way to pull representative/RefSeq genome using full species name?
2.8 years ago by
LChart
5.1k
0
votes
1
reply
1.0k
views
Comment:
Comment: How to convert abundance table to mean ranked abundance table in R
2.8 years ago by
LChart
5.1k
1
vote
0
replies
1.3k
views
Comment:
Comment: Gene Tracks from 10x Data
2.8 years ago by
LChart
5.1k
0
votes
1
reply
2.1k
views
Comment:
Comment: Box plots with logFC values
2.8 years ago by
LChart
5.1k
0
votes
0
replies
1.5k
views
Answer:
Answer: Brain cell type deconvolution
2.8 years ago by
LChart
5.1k
0
votes
0
replies
1.6k
views
Comment:
Comment: Index files from alignments are always 96 bytes (Oxford Nanopore)
2.8 years ago by
LChart
5.1k
620 results • Page
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