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Comment: Comment: Forum: Cataloguing available spatial transcriptomics tools, then linking them to
3 months ago by LauferVA 4.2k
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Comment: Comment: Extracting LOF variants and incidence from GnomAD for a list of genes
3 months ago by LauferVA 4.2k
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1.3k
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Comment: Comment: Some lines are not well organized in BED file, how to correct them ? Thanks a lo
3 months ago by LauferVA 4.2k
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1.3k
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Comment: Comment: Some lines are not well organized in BED file, how to correct them ? Thanks a lo
3 months ago by LauferVA 4.2k
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628
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Comment: Comment: pVCF versus gVCF
3 months ago by LauferVA 4.2k
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1.0k
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Comment: Comment: sc-RNA seq pipeline
3 months ago by LauferVA 4.2k
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613
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Comment: Comment: ICD9 versus ID10 in UK BRAP
3 months ago by LauferVA 4.2k
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1.0k
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Comment: Comment: sc-RNA seq pipeline
3 months ago by LauferVA 4.2k
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673
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Comment: Comment: VCF heterozygosity
3 months ago by LauferVA 4.2k
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971
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Comment: Comment: HGVS Nomenclature of Multiple Indels found in Cis
4 months ago by LauferVA 4.2k
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971
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Comment: Comment: HGVS Nomenclature of Multiple Indels found in Cis
4 months ago by LauferVA 4.2k
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971
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Comment: Comment: HGVS Nomenclature of Multiple Indels found in Cis
4 months ago by LauferVA 4.2k
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372
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Comment: Comment: what is the best way to build my design model with DESeq2
4 months ago by LauferVA 4.2k
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8.8k
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Comment: Comment: ChatGPT optimized for bioinformatics questions
4 months ago by LauferVA 4.2k
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Comment: Comment: What are the methods to correlate/study metabolomics data to proteomics data?
4 months ago by LauferVA 4.2k
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8.8k
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Comment: Comment: ChatGPT optimized for bioinformatics questions
4 months ago by LauferVA 4.2k
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774
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Comment: Comment: which statistical test and which package for comapre datasets?
4 months ago by LauferVA 4.2k
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774
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Comment: Comment: which statistical test and which package for comapre datasets?
4 months ago by LauferVA 4.2k
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Comment: Comment: Software for Spatial Transcriptomic data [NanoString; Visium]?
4 months ago by LauferVA 4.2k
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1.2k
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Comment: Comment: Is my data too noisy for DESeq? Should I model noise as unwanted variation?
5 months ago by LauferVA 4.2k
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1.2k
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Comment: Comment: Is my data too noisy for DESeq? Should I model noise as unwanted variation?
5 months ago by LauferVA 4.2k
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1.2k
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Comment: Comment: Is my data too noisy for DESeq? Should I model noise as unwanted variation?
5 months ago by LauferVA 4.2k
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1.2k
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Comment: Comment: Is my data too noisy for DESeq? Should I model noise as unwanted variation?
5 months ago by LauferVA 4.2k
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589
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Comment: Comment: Indexing pubmed articles by data available?
5 months ago by LauferVA 4.2k
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589
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Comment: Comment: Indexing pubmed articles by data available?
5 months ago by LauferVA 4.2k
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865
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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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675
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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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501
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Comment: Comment: Scanning for ultra-hot topics in science via pubmed, or using other tools
7 months ago by LauferVA 4.2k
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1.4k
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Comment: Comment: Inflated GWAS test statistic after merging multiple batches of genotype dataset
7 months ago by LauferVA 4.2k
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1.4k
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Comment: Comment: Inflated GWAS test statistic after merging multiple batches of genotype dataset
7 months ago by LauferVA 4.2k
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740
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Comment: Comment: Create 10,000bp windows for a SNP file and assign each SNP to its respective win
7 months ago by LauferVA 4.2k
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924
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Comment: Comment: For high quality Telomere to telomere assemblies, is short read polishing still
7 months ago by LauferVA 4.2k
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1.1k
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Comment: Comment: Normalization for microarrays >1000+ samples?
7 months ago by LauferVA 4.2k
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1.1k
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Comment: Comment: Normalization for microarrays >1000+ samples?
7 months ago by LauferVA 4.2k
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1.1k
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Comment: Comment: Normalization for microarrays >1000+ samples?
7 months ago by LauferVA 4.2k
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652
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Comment: Comment: SNPs that have the same position and alleles, which rsnumber to pick?
7 months ago by LauferVA 4.2k
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652
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Comment: Comment: SNPs that have the same position and alleles, which rsnumber to pick?
7 months ago by LauferVA 4.2k
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736
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Comment: Comment: The effect of SNPs at the same location
7 months ago by LauferVA 4.2k
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5.2k
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Comment: Comment: ISCN annotation for SV/CN VCF files
7 months ago by LauferVA 4.2k
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515
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Comment: Comment: WGCNA
7 months ago by LauferVA 4.2k
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795
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Comment: Comment: How to determine number of SNPs called?
8 months ago by LauferVA 4.2k
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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
8 months ago by LauferVA 4.2k
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698
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Comment: Comment: CNV benchmarking
8 months ago by LauferVA 4.2k
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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
8 months ago by LauferVA 4.2k
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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
8 months ago by LauferVA 4.2k
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763
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Comment: Comment: Pipeline Generator
8 months ago by LauferVA 4.2k
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1.2k
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Comment: Comment: Tool to search for missing genes among genome annotation versions?
8 months ago by LauferVA 4.2k
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1.2k
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Comment: Comment: Tool to search for missing genes among genome annotation versions?
8 months ago by LauferVA 4.2k
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827
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Comment: Comment: is it correct to normalize batch corrected data?
8 months ago by LauferVA 4.2k
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1.2k
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Comment: Comment: Tool to search for missing genes among genome annotation versions?
8 months ago by LauferVA 4.2k
475 results • Page 2 of 10
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