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Comment: Comment: Is my data too noisy for DESeq? Should I model noise as unwanted variation?
6 months ago by LauferVA 4.2k
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1.3k
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Comment: Comment: Is my data too noisy for DESeq? Should I model noise as unwanted variation?
6 months ago by LauferVA 4.2k
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2
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1.3k
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Comment: Comment: Is my data too noisy for DESeq? Should I model noise as unwanted variation?
6 months ago by LauferVA 4.2k
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622
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Comment: Comment: Indexing pubmed articles by data available?
6 months ago by LauferVA 4.2k
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622
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Comment: Comment: Indexing pubmed articles by data available?
6 months ago by LauferVA 4.2k
1
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4
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622
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Indexing pubmed articles by data available?
search data pubmed query
6 months ago by LauferVA 4.2k
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0
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945
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Comment: Comment: How to 'organize' multiple umap/genes generates with Seurat `FeaturePlot`in a sp
6 months ago by LauferVA 4.2k
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706
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Comment: Comment: Enrichment of mitochondrial and ribosomal pathways - an artifact?
7 months ago by LauferVA 4.2k
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356
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Current landscape of approaches to scRNA-seq with nanopore sequencers?
scRNA-seq nanopore single-cell
7 months ago by LauferVA 4.2k
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0
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524
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Comment: Comment: Scanning for ultra-hot topics in science via pubmed, or using other tools
8 months ago by LauferVA 4.2k
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1.5k
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Comment: Comment: Inflated GWAS test statistic after merging multiple batches of genotype dataset
8 months ago by LauferVA 4.2k
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0
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1.5k
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Comment: Comment: Inflated GWAS test statistic after merging multiple batches of genotype dataset
8 months ago by LauferVA 4.2k
2
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1
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1.5k
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Answer: Answer: Inflated GWAS test statistic after merging multiple batches of genotype dataset
8 months ago by LauferVA 4.2k
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0
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773
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Comment: Comment: Create 10,000bp windows for a SNP file and assign each SNP to its respective win
8 months ago by LauferVA 4.2k
3
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2
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524
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Scanning for ultra-hot topics in science via pubmed, or using other tools
growth pubmed
8 months ago by LauferVA 4.2k
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1
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973
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Comment: Comment: For high quality Telomere to telomere assemblies, is short read polishing still
8 months ago by LauferVA 4.2k
1
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0
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973
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Answer: Answer: For high quality Telomere to telomere assemblies, is short read polishing still
8 months ago by LauferVA 4.2k
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0
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1.2k
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Comment: Comment: Normalization for microarrays >1000+ samples?
8 months ago by LauferVA 4.2k
0
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1
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1.2k
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Comment: Comment: Normalization for microarrays >1000+ samples?
8 months ago by LauferVA 4.2k
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1
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1.2k
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Comment: Comment: Normalization for microarrays >1000+ samples?
8 months ago by LauferVA 4.2k
1
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0
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682
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Comment: Comment: SNPs that have the same position and alleles, which rsnumber to pick?
8 months ago by LauferVA 4.2k
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1
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682
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Comment: Comment: SNPs that have the same position and alleles, which rsnumber to pick?
8 months ago by LauferVA 4.2k
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1
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763
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Comment: Comment: The effect of SNPs at the same location
8 months ago by LauferVA 4.2k
2
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6.6k
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Comment: Comment: ISCN annotation for SV/CN VCF files
8 months ago by LauferVA 4.2k
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6.6k
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Answer: Answer: ISCN annotation for SV/CN VCF files
6 weeks ago by LauferVA 4.2k
0
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0
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535
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Comment: Comment: WGCNA
8 months ago by LauferVA 4.2k
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1
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826
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Comment: Comment: How to determine number of SNPs called?
8 months ago by LauferVA 4.2k
1
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1
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1.3k
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Comment: Comment: the distribution of log2Fc and t value are not similar for bulk RNA-seq
9 months ago by LauferVA 4.2k
1
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0
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822
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Answer: Answer: Why do the same genetic variants sometimes result in different amino acids in th
9 months ago by LauferVA 4.2k
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1
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732
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Comment: Comment: CNV benchmarking
9 months ago by LauferVA 4.2k
1
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0
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1.3k
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Comment: Comment: the distribution of log2Fc and t value are not similar for bulk RNA-seq
9 months ago by LauferVA 4.2k
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0
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1.3k
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Comment: Comment: the distribution of log2Fc and t value are not similar for bulk RNA-seq
9 months ago by LauferVA 4.2k
0
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0
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783
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Comment: Comment: Pipeline Generator
9 months ago by LauferVA 4.2k
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0
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1.2k
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Comment: Comment: Tool to search for missing genes among genome annotation versions?
9 months ago by LauferVA 4.2k
2
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1
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754
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Answer: Answer: how to check if DE genes are enriched in custom genomic regions derived from epi
9 months ago by LauferVA 4.2k
0
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1
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1.2k
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Comment: Comment: Tool to search for missing genes among genome annotation versions?
9 months ago by LauferVA 4.2k
0
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0
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882
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Comment: Comment: is it correct to normalize batch corrected data?
9 months ago by LauferVA 4.2k
3
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1.1k
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Answer: Answer: t-SNE plot dots that are close together assigned to different clusters.
9 months ago by LauferVA 4.2k
0
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0
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1.2k
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Comment: Comment: Tool to search for missing genes among genome annotation versions?
9 months ago by LauferVA 4.2k
0
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1
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828
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Comment: Comment: how to compare mapping of WES samples to human pangenome?
9 months ago by LauferVA 4.2k
0
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1
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1.2k
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Comment: Comment: Tool to search for missing genes among genome annotation versions?
9 months ago by LauferVA 4.2k
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1
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519
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Comment: Comment: list all drugs for a specific indication in ChEMBL webpage or API
9 months ago by LauferVA 4.2k
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1
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1.4k
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Comment: Comment: Revisit where to find CCLE RNAseq in FPKM or RPKM using RSEM values to perfo
9 months ago by LauferVA 4.2k
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1
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837
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Comment: Comment: plink QC
9 months ago by LauferVA 4.2k
2
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1
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837
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Answer: Answer: plink QC
9 months ago by LauferVA 4.2k
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1.5k
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Comment: Comment: How can I generate a list of 100 genomic intervals from bam files?
9 months ago by LauferVA 4.2k
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0
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663
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Comment: Comment: Abnormalties regarding the use of HPC02 (a CPU server from the school) server fo
9 months ago by LauferVA 4.2k
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0
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663
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Answer: Answer: Abnormalties regarding the use of HPC02 (a CPU server from the school) server fo
9 months ago by LauferVA 4.2k
0
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1
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1.5k
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Answer: Answer: How can I generate a list of 100 genomic intervals that are 100kb long and in wh
9 months ago by LauferVA 4.2k
0
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1
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958
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Comment: Comment: How to find gene id and gene name after I know rsid
9 months ago by LauferVA 4.2k
742 results • Page 3 of 15
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