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  2. Template:NCBI RefSeq - Wikipedia

    en.wikipedia.org/wiki/Template:NCBI_RefSeq

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  3. RefSeq - Wikipedia

    en.wikipedia.org/wiki/RefSeq

    Several projects to improve RefSeq services are currently in development by the NCBI, often in collaboration with research centers such as EMBL-EBI: . Consensus CDS (CCDS): This project aims to identify a core set of human and mouse protein-coding regions and standardize sets of genes with high and consistent levels of genomic annotation quality.

  4. Template:RefSeq - Wikipedia

    en.wikipedia.org/wiki/Template:RefSeq

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  5. National Center for Biotechnology Information - Wikipedia

    en.wikipedia.org/wiki/National_Center_for...

    Protein database maintains the text record for individual protein sequences, derived from many different resources such as NCBI Reference Sequence (RefSeq) project, GenBank, PDB, and UniProtKB/SWISS-Prot. Protein records are present in different formats including FASTA and XML and are linked to other NCBI resources. Protein provides the ...

  6. FASTA format - Wikipedia

    en.wikipedia.org/wiki/FASTA_format

    This allows a sequence that was obtained from a database to be labelled with a reference to its database record. The database identifier format is understood by the NCBI tools like makeblastdb and table2asn. The following list describes the NCBI FASTA defined format for sequence identifiers. [9]

  7. Template:NCBI - Wikipedia

    en.wikipedia.org/wiki/Template:NCBI

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  8. Reference genome - Wikipedia

    en.wikipedia.org/wiki/Reference_genome

    The first printout of the human reference genome presented as a series of books, displayed at the Wellcome Collection, London. A reference genome (also known as a reference assembly) is a digital nucleic acid sequence database, assembled by scientists as a representative example of the set of genes in one idealized individual organism of a species.

  9. List of sequence alignment software - Wikipedia

    en.wikipedia.org/wiki/List_of_sequence_alignment...

    Slider is an application for the Illumina Sequence Analyzer output that uses the "probability" files instead of the sequence files as an input for alignment to a reference sequence or a set of reference sequences. Yes Yes No No [53] [54] 2009-2010 SOAP, SOAP2, SOAP3, SOAP3-dp SOAP: robust with a small (1-3) number of gaps and mismatches.