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Comment: C: worm base genes biomaRt filter
8.7 years ago by BruceB ▴ 350
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Job: Bioinformatician - WormBase ParaSite at Sanger Institute, Cambridge
WormBase
updated 2.2 years ago by 45k • written 8.8 years ago by ▴ 350
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Job: Bioinformatician (Cancer Genomics Group) In London, Uk
ngs cancer-genomics
updated 2.3 years ago by 45k • written 11.4 years ago by ▴ 350
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Answer: A: How Can I Find Out Unknown Illumina Barcode.
11.4 years ago by BruceB ▴ 350
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Comment: C: Complete Genomic Vcf File
11.5 years ago by BruceB ▴ 350
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Answer: A: Book Recommendations For Genomics?
11.5 years ago by BruceB ▴ 350
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5.2k
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Comment: C: 1000G Query / Using Tabix With A Proxy
11.5 years ago by BruceB ▴ 350
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5.2k
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Comment: C: 1000G Query / Using Tabix With A Proxy
11.5 years ago by BruceB ▴ 350
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3.3k
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Answer: A: Bitwise Flag Samtools
11.6 years ago by BruceB ▴ 350
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10k
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Best Tool For Aligning Short Sequence Against Genome
short sequence alignment
updated 11.6 years ago by ★ 2.7k • written 11.7 years ago by ▴ 350
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Comment: C: Thorough Documentation Of Samtools Flagstat
11.7 years ago by BruceB ▴ 350
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6.8k
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Answer: A: Thorough Documentation Of Samtools Flagstat
11.7 years ago by BruceB ▴ 350
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8.7k
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Comment: C: Necessary Software Package Built For Earlier Version Of R, Now What?
11.7 years ago by BruceB ▴ 350
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10k
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Comment: C: Best Tool For Aligning Short Sequence Against Genome
11.7 years ago by BruceB ▴ 350
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30k
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Comment: C: Converting Gvcf Files Into Vcf
11.7 years ago by BruceB ▴ 350
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30k
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Comment: C: Converting Gvcf Files Into Vcf
11.7 years ago by BruceB ▴ 350
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30k
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Answer: A: Converting Gvcf Files Into Vcf
11.7 years ago by BruceB ▴ 350
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Answer: A: Gvcf Format From Illumina
11.7 years ago by BruceB ▴ 350
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2.8k
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Answer: A: Difference Between Target Re-Sequencing And Exome Sequencing !!
11.8 years ago by BruceB ▴ 350
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Comment: C: Next-Gen Sequencing Tutorials On Cubelp (Cranfield Bioinformatics Electronic Lea
11.8 years ago by BruceB ▴ 350
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20k
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Comment: C: Fastq Files From Different Flowcells
11.9 years ago by BruceB ▴ 350
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20k
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Answer: A: Fastq Files From Different Flowcells
11.9 years ago by BruceB ▴ 350
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4.4k
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Answer: A: Single Read Resulting In Heterozygous Snp Call In Samtools
11.9 years ago by BruceB ▴ 350
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Answer: A: Snp Calling With Bcftools Using Pileup File Format Instead Of Bcf
11.9 years ago by BruceB ▴ 350
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Answer: A: Concordance Between Ngs Snp Calls And Genotype Snp Arrays
12.1 years ago by BruceB ▴ 350
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4.9k
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Comment: C: How To Convert A Plain Squence In A Perl String Variable To Fasta Format
12.1 years ago by BruceB ▴ 350
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