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Comment: How can we be sure that this module preservation is comparing the same module ge
20 months ago by
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Comment: Annotate worm based genes
20 months ago by
Ram
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Comment: Its possible to merge GTF files from different genome versions so I can assing t
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Comment: GCP Snakemake
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Comment: GCP Snakemake
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Comment: Iterate through Seurat object to add patient information
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Comment: Iterate through Seurat object to add patient information
20 months ago by
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Comment: Iterate through Seurat object to add patient information
20 months ago by
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Comment: Iterate through Seurat object to add patient information
20 months ago by
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Comment: Error in GDCRNATools
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Comment: Help in choosing the right metric for ranking genes in fgsea
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Comment: Downstream analysis from STAR Alignment at transcript level
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Comment: I would like to exclude rRNA in RSEM and quantify it.
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Comment: learning bioinformatics
20 months ago by
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Comment: learning bioinformatics
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Comment: Values EXCEEDS the original data range after batch effect correction.
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Answer:
Answer: Cell barcode whitelists for DNBelab C Series High-throughput Single-cell RNA Ser
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Comment:
Comment: Cell barcode whitelists for DNBelab C Series High-throughput Single-cell RNA Ser
20 months ago by
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Answer: Question to order chr positions
20 months ago by
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Comment: Functional domain data from NM_ transcript id
20 months ago by
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Answer: Alignment of RNASeq with STAR for variant calling
20 months ago by
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Comment: somatic variant calling without matched normal in long-reads
20 months ago by
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Comment: Alignment of RNASeq with STAR for variant calling
20 months ago by
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Comment:
Comment: Single-cell RNA-seq: Annotation: Celltype annotation migration(mapping) with TOS
20 months ago by
Ram
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Comment: What happened to Tombo Re-squiggle
20 months ago by
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Comment: Single-cell RNA-seq: Annotation: Celltype annotation migration(mapping) with TOS
20 months ago by
Ram
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Comment: tools for closing gaps and construct a complete chromosome in Galaxy
20 months ago by
Ram
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Comment: Enrichement with clusterProfiler and biomart
20 months ago by
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Comment:
Comment: Single-cell RNA-seq: Preprocessing: Data integration and batch correction-2
20 months ago by
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1.1k
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Comment: tools for closing gaps and construct a complete chromosome in Galaxy
21 months ago by
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510
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Comment: Parameter bSubControl with no effect in dba.count?
21 months ago by
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896
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Comment: Specific error in R
21 months ago by
Ram
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Comment:
Comment: Bio-informatics Scientist at BASF | Nunhems
21 months ago by
Ram
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Comment: Single-cell RNA-seq: Annotation: Celltype auto annotation with MetaTiME
21 months ago by
Ram
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Comment:
Comment: SSR marker data
21 months ago by
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Comment: How to edit a fq.gz file
21 months ago by
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Comment: How to Use Biostars Part-3: Formatting Text and Using GitHub Gists
21 months ago by
Ram
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677
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Comment: Reference transcriptome
21 months ago by
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Comment:
Comment: How to Use Biostars Part-3: Formatting Text and Using GitHub Gists
21 months ago by
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Comment: where to work as a bioinformatician (NGS/IA)
21 months ago by
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Comment:
Comment: How to edit a fq.gz file
21 months ago by
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Comment:
Comment: fastq-dump
21 months ago by
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Comment: fastq-dump
21 months ago by
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Comment: How can I know if a gene mutation is somatic or germline?
21 months ago by
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563
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Comment:
Comment: Maximum Likelihood Phylogenetic
21 months ago by
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Answer:
Answer: How to edit a fq.gz file
21 months ago by
Ram
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3.3k
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Comment:
Comment: How to edit a fq.gz file
21 months ago by
Ram
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1.7k
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Comment:
Comment: where to work as a bioinformatician (NGS/IA)
21 months ago by
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45k
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0
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3.3k
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Comment:
Comment: How to edit a fq.gz file
21 months ago by
Ram
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987
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Comment:
Comment: Peak ranger output file
21 months ago by
Ram
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