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3
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0
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1.1k
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Answer: Answer: Batch effect correction between Bulk RNA-Seq and scRNA-Seq's clusters
23 months ago by LauferVA 4.8k
0
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0
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2.9k
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Comment: Comment: Is my data too noisy for DESeq? Should I model noise as unwanted variation?
23 months ago by LauferVA 4.8k
0
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1
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2.9k
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Comment: Comment: Is my data too noisy for DESeq? Should I model noise as unwanted variation?
23 months ago by LauferVA 4.8k
0
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1
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2.9k
views
Comment: Comment: Is my data too noisy for DESeq? Should I model noise as unwanted variation?
24 months ago by LauferVA 4.8k
0
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2
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2.9k
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Comment: Comment: Is my data too noisy for DESeq? Should I model noise as unwanted variation?
24 months ago by LauferVA 4.8k
0
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0
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1.3k
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Comment: Comment: Indexing pubmed articles by data available?
24 months ago by LauferVA 4.8k
0
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0
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1.3k
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Comment: Comment: Indexing pubmed articles by data available?
24 months ago by LauferVA 4.8k
1
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4
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1.3k
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Indexing pubmed articles by data available?
search data pubmed query
24 months ago by LauferVA 4.8k
0
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0
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2.8k
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Comment: Comment: How to 'organize' multiple umap/genes generates with Seurat `FeaturePlot`in a sp
2.0 years ago by LauferVA 4.8k
0
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0
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1.4k
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Comment: Comment: Enrichment of mitochondrial and ribosomal pathways - an artifact?
2.1 years ago by LauferVA 4.8k
0
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0
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614
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Current landscape of approaches to scRNA-seq with nanopore sequencers?
scRNA-seq nanopore single-cell
2.1 years ago by LauferVA 4.8k
0
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0
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1.0k
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Comment: Comment: Scanning for ultra-hot topics in science via pubmed, or using other tools
2.1 years ago by LauferVA 4.8k
0
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0
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3.3k
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Comment: Comment: Inflated GWAS test statistic after merging multiple batches of genotype dataset
2.1 years ago by LauferVA 4.8k
0
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0
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3.3k
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Comment: Comment: Inflated GWAS test statistic after merging multiple batches of genotype dataset
2.1 years ago by LauferVA 4.8k
2
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1
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3.3k
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Answer: Answer: Inflated GWAS test statistic after merging multiple batches of genotype dataset
2.1 years ago by LauferVA 4.8k
0
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0
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1.4k
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Comment: Comment: Create 10,000bp windows for a SNP file and assign each SNP to its respective win
2.1 years ago by LauferVA 4.8k
3
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2
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1.0k
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Scanning for ultra-hot topics in science via pubmed, or using other tools
growth pubmed
2.1 years ago by LauferVA 4.8k
0
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1
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2.6k
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Comment: Comment: For high quality Telomere to telomere assemblies, is short read polishing still
2.1 years ago by LauferVA 4.8k
1
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0
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2.6k
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Answer: Answer: For high quality Telomere to telomere assemblies, is short read polishing still
2.1 years ago by LauferVA 4.8k
0
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0
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2.2k
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Comment: Comment: Normalization for microarrays >1000+ samples?
2.1 years ago by LauferVA 4.8k
0
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1
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2.2k
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Comment: Comment: Normalization for microarrays >1000+ samples?
2.1 years ago by LauferVA 4.8k
0
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1
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2.2k
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Comment: Comment: Normalization for microarrays >1000+ samples?
2.1 years ago by LauferVA 4.8k
1
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0
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1.3k
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Comment: Comment: SNPs that have the same position and alleles, which rsnumber to pick?
2.1 years ago by LauferVA 4.8k
0
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1
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1.3k
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Comment: Comment: SNPs that have the same position and alleles, which rsnumber to pick?
2.2 years ago by LauferVA 4.8k
0
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1
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1.4k
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Comment: Comment: The effect of SNPs at the same location
2.2 years ago by LauferVA 4.8k
2
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0
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9.8k
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Comment: Comment: ISCN annotation for SV/CN VCF files
2.2 years ago by LauferVA 4.8k
1
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0
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9.8k
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Answer: Answer: ISCN annotation for SV/CN VCF files
19 months ago by LauferVA 4.8k
0
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0
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938
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Comment: Comment: WGCNA
2.2 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 determine number of SNPs called?
2.2 years ago by LauferVA 4.8k
1
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1
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2.5k
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Comment: Comment: the distribution of log2Fc and t value are not similar for bulk RNA-seq
2.2 years ago by LauferVA 4.8k
1
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0
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1.5k
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Answer: Answer: Why do the same genetic variants sometimes result in different amino acids in th
2.2 years ago by LauferVA 4.8k
0
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1
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1.5k
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Comment: Comment: CNV benchmarking
2.2 years ago by LauferVA 4.8k
1
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0
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2.5k
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Comment: Comment: the distribution of log2Fc and t value are not similar for bulk RNA-seq
2.2 years ago by LauferVA 4.8k
0
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0
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2.5k
views
Comment: Comment: the distribution of log2Fc and t value are not similar for bulk RNA-seq
2.2 years ago by LauferVA 4.8k
0
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0
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1.3k
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Comment: Comment: Pipeline Generator
2.2 years ago by LauferVA 4.8k
0
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0
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2.7k
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Comment: Comment: Tool to search for missing genes among genome annotation versions?
2.2 years ago by LauferVA 4.8k
2
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1
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1.4k
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Answer: Answer: how to check if DE genes are enriched in custom genomic regions derived from epi
2.2 years ago by LauferVA 4.8k
0
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1
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2.7k
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Comment: Comment: Tool to search for missing genes among genome annotation versions?
2.2 years ago by LauferVA 4.8k
0
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0
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1.7k
views
Comment: Comment: is it correct to normalize batch corrected data?
2.2 years ago by LauferVA 4.8k
3
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0
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2.5k
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Answer: Answer: t-SNE plot dots that are close together assigned to different clusters.
2.2 years ago by LauferVA 4.8k
0
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0
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2.7k
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Comment: Comment: Tool to search for missing genes among genome annotation versions?
2.2 years ago by LauferVA 4.8k
0
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1
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1.8k
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Comment: Comment: how to compare mapping of WES samples to human pangenome?
2.2 years ago by LauferVA 4.8k
0
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1
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2.7k
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Comment: Comment: Tool to search for missing genes among genome annotation versions?
2.2 years ago by LauferVA 4.8k
0
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1
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1.1k
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Comment: Comment: list all drugs for a specific indication in ChEMBL webpage or API
2.2 years ago by LauferVA 4.8k
0
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1
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2.5k
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Comment: Comment: Revisit where to find CCLE RNAseq in FPKM or RPKM using RSEM values to perfo
2.2 years ago by LauferVA 4.8k
0
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1
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1.8k
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Comment: Comment: plink QC
2.2 years ago by LauferVA 4.8k
2
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1
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1.8k
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Answer: Answer: plink QC
2.3 years ago by LauferVA 4.8k
1
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0
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2.6k
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Comment: Comment: How can I generate a list of 100 genomic intervals from bam files?
2.3 years ago by LauferVA 4.8k
0
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0
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1.2k
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Comment: Comment: Abnormalties regarding the use of HPC02 (a CPU server from the school) server fo
2.3 years ago by LauferVA 4.8k
0
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0
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1.2k
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Answer: Answer: Abnormalties regarding the use of HPC02 (a CPU server from the school) server fo
2.3 years ago by LauferVA 4.8k
793 results • Page 4 of 16
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