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Comment: Comment: Why my `Percent duplicates` in a shallow sequencing is too high?
3.6 years ago by LauferVA 4.8k
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2.2k
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Comment: Comment: Why my `Percent duplicates` in a shallow sequencing is too high?
3.6 years ago by LauferVA 4.8k
1
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2
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2.2k
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Answer: Answer: Why my `Percent duplicates` in a shallow sequencing is too high?
3.6 years ago by LauferVA 4.8k
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1.5k
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Comment: Comment: Genetic Model when running PCA
3.6 years ago by LauferVA 4.8k
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1.2k
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Answer: Answer: low counts in DESeq2
3.6 years ago by LauferVA 4.8k
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3.1k
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Comment: Comment: Fasta to json via python dictionary
3.6 years ago by LauferVA 4.8k
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3.1k
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Comment: Comment: Fasta to json via python dictionary
3.7 years ago by LauferVA 4.8k
1
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1.5k
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Answer: Answer: Genetic Model when running PCA
3.6 years ago by LauferVA 4.8k
1
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1
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4.7k
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Comment: Comment: WGCNA HeatMap correlating modules and sample conditions
3.7 years ago by LauferVA 4.8k
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1.2k
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Comment: Comment: How to calculate Coverage Uniformity?
3.7 years ago by LauferVA 4.8k
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1.2k
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Comment: Comment: DGE - command line alternatives to R packages?
3.7 years ago by LauferVA 4.8k
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4.7k
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Answer: Answer: WGCNA HeatMap correlating modules and sample conditions
3.7 years ago by LauferVA 4.8k
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1.4k
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Answer: Answer: Checking chromosome builds for genotyping data
3.7 years ago by LauferVA 4.8k
1
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1
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1.6k
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Comment: Comment: Alternatives to TMM normalization
3.7 years ago by LauferVA 4.8k
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751
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Answer: Answer: plink
3.7 years ago by LauferVA 4.8k
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703
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Answer: Answer: Sharing interactive Cytoscape networks
3.7 years ago by LauferVA 4.8k
2
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1.6k
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Answer: Answer: Alternatives to TMM normalization
3.7 years ago by LauferVA 4.8k
0
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0
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751
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Answer: Answer: Batch effect
3.7 years ago by LauferVA 4.8k
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1.6k
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Comment: Comment: Large number of down-regulated genes compares to upregulated genes
3.7 years ago by LauferVA 4.8k
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1.1k
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Answer: Answer: Info/r2 threshold to use for LD file for FINEMAP/SUSIE
3.7 years ago by LauferVA 4.8k
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971
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Comment: Comment: Extract first 3 PC for all confounding variables to be used as covariates
3.7 years ago by LauferVA 4.8k
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1.6k
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Comment: Comment: How to normalize and batch correct SC RNA-seq data from multiple libraries and c
3.7 years ago by LauferVA 4.8k
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679
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Different types of repeat elements in eukaryotic genomes
repeat sequence genome graph STR satellite
3.7 years ago by LauferVA 4.8k
0
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1
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1.6k
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Comment: Comment: How to normalize and batch correct SC RNA-seq data from multiple libraries and c
3.7 years ago by LauferVA 4.8k
1
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1
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1.2k
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Comment: Comment: Joint genotyping for somatic variants by using unrelated samples
3.7 years ago by LauferVA 4.8k
1
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1.2k
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Comment: Comment: How to perform imputation analysis between masked SNPs and ground truth
3.7 years ago by LauferVA 4.8k
0
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1
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4.9k
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Comment: Comment: Multiple correlations RNAseq data - correction for multiple testing?
3.7 years ago by LauferVA 4.8k
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3.3k
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Comment: Comment: How to do pathway enrichment analysis with genomic ranges data (ATAC-Seq peaks)?
3.7 years ago by LauferVA 4.8k
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960
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Comment: Comment: Cleaning up cells in clusters that clearly do not group well.
3.7 years ago by LauferVA 4.8k
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2.1k
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Comment: Comment: Existing tutorials using Docker to set up and run any type of NGS workflow?
3.7 years ago by LauferVA 4.8k
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0
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2.1k
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Comment: Comment: Existing tutorials using Docker to set up and run any type of NGS workflow?
3.7 years ago by LauferVA 4.8k
0
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1
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3.3k
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Comment: Comment: How to do pathway enrichment analysis with genomic ranges data (ATAC-Seq peaks)?
3.7 years ago by LauferVA 4.8k
0
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1
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4.9k
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Comment: Comment: Multiple correlations RNAseq data - correction for multiple testing?
3.7 years ago by LauferVA 4.8k
0
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1
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4.9k
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Comment: Comment: Multiple correlations RNAseq data - correction for multiple testing?
3.7 years ago by LauferVA 4.8k
0
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1
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4.9k
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Comment: Comment: Multiple correlations RNAseq data - correction for multiple testing?
3.7 years ago by LauferVA 4.8k
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0
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4.9k
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Comment: Comment: Multiple correlations RNAseq data - correction for multiple testing?
3.7 years ago by LauferVA 4.8k
5
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6
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2.1k
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Existing tutorials using Docker to set up and run any type of NGS workflow?
docker NGS pipeline automate workflow
3.7 years ago by LauferVA 4.8k
3
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1
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3.3k
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Answer: Answer: How to do pathway enrichment analysis with genomic ranges data (ATAC-Seq peaks)?
3.7 years ago by LauferVA 4.8k
0
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1
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5.3k
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Comment: Comment: Programmatically convert cytoband location to genomic coordinates
3.7 years ago by LauferVA 4.8k
1
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1
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4.9k
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Comment: Comment: Multiple correlations RNAseq data - correction for multiple testing?
3.7 years ago by LauferVA 4.8k
0
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1
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4.9k
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Comment: Comment: Multiple correlations RNAseq data - correction for multiple testing?
3.7 years ago by LauferVA 4.8k
0
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0
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683
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Comment: Comment: Checking correlation on raw fastq data without aligning
3.7 years ago by LauferVA 4.8k
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1
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1.3k
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Comment: Comment: How to find top-hit SNP from gwas.
3.7 years ago by LauferVA 4.8k
1
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1
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4.9k
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Comment: Comment: Multiple correlations RNAseq data - correction for multiple testing?
3.7 years ago by LauferVA 4.8k
1
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1
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1.2k
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Comment: Comment: How to perform imputation analysis between masked SNPs and ground truth
3.7 years ago by LauferVA 4.8k
0
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0
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911
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Comment: Comment: Error while running All-against-All alignments in OMA
3.7 years ago by LauferVA 4.8k
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1.4k
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Comment: Comment: Concensus functional annotation from multiple, non-redundant annotations in GFF
3.7 years ago by LauferVA 4.8k
2
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1.4k
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Comment: Comment: HPC settings for concatenating large VCF.GZ files
3.7 years ago by LauferVA 4.8k
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2.3k
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Answer: Answer: Weird QQ plot in GWAS analysis
3.7 years ago by LauferVA 4.8k
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0
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863
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Answer: Answer: Can a heterogenous approach to data normalization yield a better consensus learn
3.7 years ago by LauferVA 4.8k
793 results • Page 11 of 16
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