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Comment: C: issue running DeepMod
5.7 years ago by colindaven 8.0k
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1.6k
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Comment: C: Can a statistically associated mutation by Fisher's Exact Test, really not be as
5.7 years ago by colindaven 8.0k
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Comment: C: issue running DeepMod
5.7 years ago by colindaven 8.0k
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Answer: A: Parser for PAF to find structural variants
5.7 years ago by colindaven 8.0k
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Comment: C: Unable to map Reverse read using STAR aligner
5.7 years ago by colindaven 8.0k
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898
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Comment: C: How to create snpEff data base for newly assembled genome?
5.7 years ago by colindaven 8.0k
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Answer: A: Unable to map Reverse read using STAR aligner
5.7 years ago by colindaven 8.0k
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1.0k
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Comment: C: Non-de bruijn graph assemblers
5.7 years ago by colindaven 8.0k
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2.7k
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Answer: C: Useful productivity tools for bioinformaticians
5.8 years ago by colindaven 8.0k
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1
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7.1k
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Comment: C: Are there advantages in using high accuracy models for guppy basecaller when Ill
5.8 years ago by colindaven 8.0k
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7.1k
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Answer: A: Are there advantages in using high accuracy models for guppy basecaller when Ill
5.8 years ago by colindaven 8.0k
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1.2k
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Comment: C: Question: Best approach to bacterial hybrid genome assembly
5.8 years ago by colindaven 8.0k
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1.8k
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Restrict GTF or GFF3 to final 3' exons
rna-seq annotation
5.8 years ago by colindaven 8.0k
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0
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1.3k
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Answer: A: Visualising individual humans in RNA-seq
5.8 years ago by colindaven 8.0k
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2.2k
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Comment: C: PhD position in translational clinical implementation of metagenomics
5.9 years ago by colindaven 8.0k
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1.4k
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Answer: A: Variant using freebayes
5.9 years ago by colindaven 8.0k
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3.2k
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Answer: A: Can I split a bed file into 1000bp bins and add up my read numbers?
5.9 years ago by colindaven 8.0k
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4
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2.2k
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Job: PhD position in translational clinical implementation of metagenomics
minion bench_to_bedside ngs
updated 2.3 years ago by 45k • written 6.2 years ago by 8.0k
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2.2k
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Answer: A: PhD position in translational clinical implementation of metagenomics
5.9 years ago by colindaven 8.0k
1
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1
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7.8k
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Answer: A: Difference in R1 and R2 FASTQ files from RNA seq paired end
5.9 years ago by colindaven 8.0k
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2.6k
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Comment: C: Spades has been running for over a week. Normal?
5.9 years ago by colindaven 8.0k
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3.4k
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Comment: C: What is in your opinion the current state-of-the-art sequencing platform for gen
5.9 years ago by colindaven 8.0k
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957
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Answer: A: snpEff Apis_mellifera genome
5.9 years ago by colindaven 8.0k
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1
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6.0k
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Comment: C: GPU based parallel processing in genomics tools
5.9 years ago by colindaven 8.0k
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1
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3.2k
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Comment: C: Allelic-Specific RNA-Seq pipeline
5.9 years ago by colindaven 8.0k
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6.0k
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Answer: A: GPU based parallel processing in genomics tools
5.9 years ago by colindaven 8.0k
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3.2k
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Comment: C: Allelic-Specific RNA-Seq pipeline
5.9 years ago by colindaven 8.0k
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4.2k
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Comment: C: Bioinformatician, a jack of all trades, but in the eye of the CV-beholder a mast
5.9 years ago by colindaven 8.0k
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0
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1.8k
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Comment: C: workstation purchase for metadata analysis and running guppy
6.0 years ago by colindaven 8.0k
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1.8k
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Comment: C: workstation purchase for metadata analysis and running guppy
6.0 years ago by colindaven 8.0k
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2
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1.8k
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Answer: A: workstation purchase for metadata analysis and running guppy
6.0 years ago by colindaven 8.0k
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1
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3.1k
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Comment: C: How do you assemble contigs without using a reference genome?
6.0 years ago by colindaven 8.0k
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1
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1.6k
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Answer: A: What's the best practice to do scaffolding?
6.0 years ago by colindaven 8.0k
4
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1
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5.4k
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Answer: A: Shotgun metagenomics high duplication read rate - how high is too high?
6.0 years ago by colindaven 8.0k
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3.4k
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Comment: C: Generate GTF/GFF file (coordinates) from a FASTA annotated file.
6.0 years ago by colindaven 8.0k
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1
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4.0k
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Comment: C: Would this laptop be futureproof for bioinformatics work
6.0 years ago by colindaven 8.0k
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1
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13k
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Comment: C: Using the MinION MinKNOW software on Ubuntu 1604
6.1 years ago by colindaven 8.0k
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3.6k
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Comment: C: Good coverage value for de novo assembly with NanoPore Reads?
6.1 years ago by colindaven 8.0k
0
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1
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1.9k
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Comment: C: High CDS Count in my assembled Genome using Nanopore reads (ONT) data
6.1 years ago by colindaven 8.0k
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2.1k
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Comment: C: Pipeline for SNP analysis
6.1 years ago by colindaven 8.0k
1
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0
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14k
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Answer: A: Genome assembly statistical tools
6.1 years ago by colindaven 8.0k
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2.6k
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Comment: C: I can't see my bam file on igv
6.1 years ago by colindaven 8.0k
1
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1
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1.4k
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Answer: A: Predicted Proteins: Mapping Reads to ORFs
6.1 years ago by colindaven 8.0k
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1
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1.4k
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Comment: C: E coli Illumina paired assembly using a reference genome?
6.1 years ago by colindaven 8.0k
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Answer: A: Assembler suggestions for ~90Mb genome (using single-end Illumina & PacBio data
6.2 years ago by colindaven 8.0k
1
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0
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1.3k
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Answer: A: Freebayes haplotype calling
6.2 years ago by colindaven 8.0k
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1
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1.2k
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Comment: C: Placing SNPs within updated genome assembly
6.2 years ago by colindaven 8.0k
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1
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1.5k
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Comment: C: BioNano fasta file formatting issue
6.2 years ago by colindaven 8.0k
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2.4k
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Answer: A: How to evaluate sequence alignment (e.g. number of indels) of ONT data after dat
6.2 years ago by colindaven 8.0k
1
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1.4k
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Answer: A: How to Analyze Overlapping Peaks using ChIP-Seq Data
6.2 years ago by colindaven 8.0k
1,105 results • Page 17 of 23
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