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1.3k
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Comment: C: transcriptomics gene expression per sample
5.4 years ago by igor 13k
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1.3k
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Comment: C: transcriptomics gene expression per sample
5.4 years ago by igor 13k
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1
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3.6k
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Answer: A: 10x Single cell data analysis with Monocle
5.4 years ago by igor 13k
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Answer: A: Is there a single cell RNAseq equivalent of GTEx or TCGA?
5.4 years ago by igor 13k
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2.8k
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Comment: C: PanCancerAtlas RNA-SeqV2 (RSEM) file contains negative values
5.4 years ago by igor 13k
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1.8k
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Comment: C: Doubt regarding dna sequence length
5.4 years ago by igor 13k
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14k
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Answer: A: TMB Tumor Mutation Burden
5.4 years ago by igor 13k
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1.7k
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Answer: A: RNA-seq data for binary classification problem
5.4 years ago by igor 13k
2
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4.0k
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Answer: A: Which programming langauge shall I start as a beginner in Bioinformatics
5.4 years ago by igor 13k
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1
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4.0k
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Comment: C: Which programming langauge shall I start as a beginner in Bioinformatics
5.4 years ago by igor 13k
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3.8k
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Comment: C: Amazon AWS setup for the bioinformatic analysis particularly scRNAseq
5.4 years ago by igor 13k
1
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14k
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Comment: C: TMB Tumor Mutation Burden
5.4 years ago by igor 13k
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1.7k
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Comment: C: DEG analysis when not replicates are available
5.4 years ago by igor 13k
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1
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1.5k
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Comment: C: Filter SNPs for DP using mean + 2*SD
5.4 years ago by igor 13k
1
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2
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1.7k
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Comment: C: DEG analysis when not replicates are available
5.4 years ago by igor 13k
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5.1k
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Comment: C: question about 10X sc-RNA-seq
5.4 years ago by igor 13k
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10k
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Comment: C: Cellranger aggr versus Seurat
5.4 years ago by igor 13k
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2
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5.1k
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Comment: C: question about 10X sc-RNA-seq
5.4 years ago by igor 13k
1
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1
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10k
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Answer: A: Cellranger aggr versus Seurat
5.4 years ago by igor 13k
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948
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Comment: C: Do tools doing clonal evolution analysis work on unmatched samples too
5.4 years ago by igor 13k
1
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1
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948
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Answer: C: Do tools doing clonal evolution analysis work on unmatched samples too
5.4 years ago by igor 13k
1
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1
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1.6k
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Answer: A: Seurat - weird behavior in the counts object.
5.4 years ago by igor 13k
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12k
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Comment: C: Analyzing digital gene expression data (DGE) from drop-seq pipeline with Seurat.
5.4 years ago by igor 13k
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1.3k
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Answer: C: What is the best approach to normalize exon read counts between samples ?
5.4 years ago by igor 13k
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1
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23k
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Comment: C: bcl2fastq2: how to correctly use the --use-bases-mask for different sequencing m
5.4 years ago by igor 13k
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1
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23k
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Comment: C: bcl2fastq2: how to correctly use the --use-bases-mask for different sequencing m
5.4 years ago by igor 13k
1
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2.8k
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Answer: C: cellRanger 2.0 to Seurat 3.1.2
5.4 years ago by igor 13k
1
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1.7k
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Comment: C: Comparing datasets from two different library methods
5.4 years ago by igor 13k
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1
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8.4k
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Comment: C: about batch correction in scRNA-seq
5.5 years ago by igor 13k
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1
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1.7k
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Comment: C: Comparing datasets from two different library methods
5.5 years ago by igor 13k
0
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1
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1.7k
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Comment: C: Comparing datasets from two different library methods
5.5 years ago by igor 13k
1
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1.1k
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Comment: C: LncRNA and Immune-related genes
5.5 years ago by igor 13k
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3.5k
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Comment: C: Reference mouse genome
5.5 years ago by igor 13k
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1
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1.1k
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Comment: C: Target capture sequencing
5.5 years ago by igor 13k
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0
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2.2k
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Comment: C: Processing bulk RNA-seq TMM matrix to get DEGs
5.5 years ago by igor 13k
1
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1
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9.6k
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Comment: C: Store a scRNA-seq ~gene expression "matrix.txt" as a "matrix.mtx" in R
5.5 years ago by igor 13k
0
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1
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2.2k
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Comment: C: Processing bulk RNA-seq TMM matrix to get DEGs
5.5 years ago by igor 13k
1
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1
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2.8k
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Comment: C: Run Cellranger Count with Novogene fastq files
5.5 years ago by igor 13k
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3.8k
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Comment: C: single cell RNA seq Differential Expression using MAST
5.5 years ago by igor 13k
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1.5k
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Comment: C: MD5 not the same between contig and reference; both Unified Genotyper and Haplot
5.5 years ago by igor 13k
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0
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12k
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Comment: C: GTF/GFF for non-coding RNA
5.5 years ago by igor 13k
1
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1
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1.5k
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Answer: A: MD5 not the same between contig and reference; both Unified Genotyper and Haplot
5.5 years ago by igor 13k
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0
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1.4k
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Comment: C: free linux server
5.5 years ago by igor 13k
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0
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2.2k
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Comment: C: R Package for Visualizing SNVs from "sites only" VCF (population variants)
5.5 years ago by igor 13k
0
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1
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2.2k
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Comment: C: R Package for Visualizing SNVs from "sites only" VCF (population variants)
5.5 years ago by igor 13k
1
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1
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1.4k
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Comment: C: Extract RNA Support for Somatic SNV Identified using DNA
5.5 years ago by igor 13k
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1
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1.4k
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Comment: C: Extract RNA Support for Somatic SNV Identified using DNA
5.5 years ago by igor 13k
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2.1k
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Comment: C: What causes strange oscillations in the count distribution of Salmon and STAR al
5.5 years ago by igor 13k
1
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1
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2.1k
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Comment: C: What causes strange oscillations in the count distribution of Salmon and STAR al
5.5 years ago by igor 13k
0
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0
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2.1k
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Comment: C: What causes strange oscillations in the count distribution of Salmon and STAR al
5.5 years ago by igor 13k
1,531 results • Page 7 of 31
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