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Comment: Comment: Visualization package for Maf Files using Python
2.0 years ago by Mark ★ 1.7k
0
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1
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2.3k
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Comment: Comment: Aligner with statistics included?
2.0 years ago by Mark ★ 1.7k
0
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1
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1.6k
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Comment: Comment: Why 99% at 20X for sequencing?
2.0 years ago by Mark ★ 1.7k
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2
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2.1k
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Comment: Comment: Filtering a 10X generated .bam file based on a list of barcodes
2.0 years ago by Mark ★ 1.7k
1
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1
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3.0k
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Comment: Comment: Annotating Proteins in heatmap with 1 or more pathways using R.
2.0 years ago by Mark ★ 1.7k
1
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0
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3.0k
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Comment: Comment: Annotating Proteins in heatmap with 1 or more pathways using R.
2.0 years ago by Mark ★ 1.7k
2
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1
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3.0k
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Answer: Answer: Annotating Proteins in heatmap with 1 or more pathways using R.
2.0 years ago by Mark ★ 1.7k
1
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1
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6.2k
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Comment: Comment: Which alignment for whole bacterial genomes for phylogenetic tree?
2.0 years ago by Mark ★ 1.7k
1
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1
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3.0k
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Comment: Comment: Annotating Proteins in heatmap with 1 or more pathways using R.
2.0 years ago by Mark ★ 1.7k
1
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0
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2.3k
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Answer: Answer: GSEApy plot TypeError
updated 23 months ago by 45k • written 2.1 years ago by ★ 1.7k
0
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0
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2.2k
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Answer: Answer: Extract compounds/proteins from genomic data
2.1 years ago by Mark ★ 1.7k
0
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0
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1.2k
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Comment: Comment: How to read tsv data as dgcmatrix
2.1 years ago by Mark ★ 1.7k
1
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0
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1.6k
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Comment: Comment: how to get to a VCF from bam files
2.1 years ago by Mark ★ 1.7k
1
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1
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1.4k
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Comment: Comment: KEGG Pathway analysis for non-model organism using goseq
2.1 years ago by Mark ★ 1.7k
0
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1
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1.8k
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Comment: Comment: pyDESeq2 Index Error?
2.1 years ago by Mark ★ 1.7k
1
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0
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910
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Answer: Answer: Visualization of Genomes
2.1 years ago by Mark ★ 1.7k
2
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1
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2.2k
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Answer: Answer: vcf.gz to vcf
2.1 years ago by Mark ★ 1.7k
1
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0
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1.4k
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Answer: Answer: How to get ncol = nrow?
updated 2.1 years ago by 45k • written 2.1 years ago by ★ 1.7k
1
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0
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1.8k
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Comment: Comment: Viewing chromatograms on linux
2.1 years ago by Mark ★ 1.7k
2
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0
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1.8k
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Answer: Answer: Viewing chromatograms on linux
2.1 years ago by Mark ★ 1.7k
2
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0
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16k
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Answer: Answer: find positions of a short sequence in a genome
2.2 years ago by Mark ★ 1.7k
0
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0
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3.5k
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Comment: Comment: Problem with mamba/conda install
2.3 years ago by Mark ★ 1.7k
0
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1
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1.0k
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Comment: Comment: Chewbbaca - explanation of the output
2.3 years ago by Mark ★ 1.7k
1
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0
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1.1k
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Comment: Comment: Download rRNAs.fasta for all bacteria from database
2.3 years ago by Mark ★ 1.7k
0
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0
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3.5k
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Comment: Comment: I want to rename sequence headers
2.3 years ago by Mark ★ 1.7k
1
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0
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2.0k
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Answer: Answer: Best pipeline / resources / tools for whole genome assembly
2.3 years ago by Mark ★ 1.7k
3
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2
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2.8k
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Answer: Answer: adding features to gtf file using agat tool function
2.3 years ago by Mark ★ 1.7k
1
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1
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3.5k
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Answer: Answer: I want to rename sequence headers
2.3 years ago by Mark ★ 1.7k
0
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1
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1.3k
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Comment: Comment: How do I calculate differential expression for RNA-seq values with the "limma" p
2.4 years ago by Mark ★ 1.7k
0
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0
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1.8k
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Comment: Comment: Reorder GO terms using R
2.4 years ago by Mark ★ 1.7k
0
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1
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1.1k
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Answer: Answer: how to look at interaction between SNP and gene
2.6 years ago by Mark ★ 1.7k
1
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0
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1.1k
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Answer: Answer: Remove part of headers in FASTA file
2.6 years ago by Mark ★ 1.7k
1
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0
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1.2k
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Answer: Answer: Merging Contigs
2.8 years ago by Mark ★ 1.7k
0
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0
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1.4k
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Comment: Comment: Concepts reg Zygosity, copy number variant and variation
2.8 years ago by Mark ★ 1.7k
1
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0
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5.6k
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Answer: Answer: DoubletFinder for Python?
2.8 years ago by Mark ★ 1.7k
0
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0
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1.6k
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Comment: Comment: bedtools intersect VCF with BED Invalid record error.
3.0 years ago by Mark ★ 1.7k
1
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1
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1.4k
views
Comment: Comment: Concepts reg Zygosity, copy number variant and variation
3.0 years ago by Mark ★ 1.7k
0
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1
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1.8k
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Comment: Comment: Cellranger find which fastq file every cell belongs to
3.0 years ago by Mark ★ 1.7k
0
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1
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950
views
Comment: Comment: bowtie2-build --noauto parameter
updated 2.9 years ago by 45k • written 3.0 years ago by ★ 1.7k
3
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0
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1.3k
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Answer: Answer: extracting contigs
3.0 years ago by Mark ★ 1.7k
0
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0
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745
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Comment: Comment: MLST to Serotype
3.2 years ago by Mark ★ 1.7k
0
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1
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1.4k
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Comment: Comment: Correlogram under barplot
3.2 years ago by Mark ★ 1.7k
1
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1
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1.6k
views
Comment: Comment: Mapping GeneSymbol plus cDNA position to a Chr:Position ... without transcript I
3.2 years ago by Mark ★ 1.7k
1
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0
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1.0k
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Answer: Answer: Generate consensus sequence without considering gaps
3.2 years ago by Mark ★ 1.7k
0
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0
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1.8k
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Comment: Comment: edgeR glmRT code error message
3.2 years ago by Mark ★ 1.7k
0
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0
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857
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Answer: Answer: how to create a dataset from fastq sequence files in ubuntu
3.4 years ago by Mark ★ 1.7k
0
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1
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2.8k
views
Comment: Comment: Making a pheatmap legend with superscripts
3.4 years ago by Mark ★ 1.7k
1
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0
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1.7k
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Comment: Comment: Specific case of "bedtools intersect"
3.5 years ago by Mark ★ 1.7k
1
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0
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1.2k
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Comment: Comment: Multiple file genome alignment with STAR
3.5 years ago by Mark ★ 1.7k
0
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0
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2.6k
views
Answer: Answer: How can I use ggplot2 to indicate chromosomes on a continuous axis?
3.6 years ago by Mark ★ 1.7k
344 results • Page 2 of 7
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