Tags

A tag is a keyword or label that categorizes your question with other, similar questions. Using the right tags makes it easier for others to find and answer your question.

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Short nucleotide sequence used by many sequencing methods in order to amplify DNA/RNA fragments, identify DNA/RNA fragments uniquely (Unique Molecular Identifier), anchor DNA/RNA fragments to the flow…
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These questions are about sequence alignment.
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Allele frequency is the foundational basis of the vast majority of population genetic calculations
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Power all inclusive package used in data science for managing Python and its dependencies
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The process of attaching contextual information to a biomolecular (DNA, RNA, or protein) sequence, such as the location of genes, promoters, or repeats in genomic DNA, or the function of a protein.
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Process of creating the original sequence from the read sequences that it generated during a sequencing experiment. Can refer to genome assembly, in which case the original sequence is a genome, or tr…
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Acronym for Amazon Webservices
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One of the three domains of life, with Archaea and eukaryotes. Bacteria, along with Archaea, are prokaryotes, i.e. lack a nucleus.
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The "Binary Alignment Map" (BAM) format is one of the common binary formats used to store sequence alignment information. Questions should include this tag if they directly pertain to the format itsel…
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The process of transforming the raw signal of a sequencer (light, images, electrical signal) into DNA or RNA bases. For Illumina, the basecalling consists of transforming the pictures with lights of d…
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The removal of bases at the end of reads to make an alignment better.
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to refer to the questions related to the Linux and Unix shell abbreviated as bash (Bourne Again SHell). It has notable programmatic strengths over C shell (csh) and touch C shell (tcsh)
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Phylogenetics package based on Bayesian statistics often used in molecular clock calculation
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Browser Extensible Data, a collection of related plain text formats for describing genome features for visualization with genome browsers.
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