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  2. De novo peptide sequencing - Wikipedia

    en.wikipedia.org/wiki/De_novo_peptide_sequencing

    Then continue to identify y n-2, y n-3... ions by matching mass differences with the amino acid residue masses (see Table 1). Look for the corresponding b-ions of the identified y-ions. The mass of b+y ions is the mass of the peptide +2 Da. After identifying the y-ion series and b-ion series, assign the amino acid sequence and check the mass.

  3. Leroy Hood - Wikipedia

    en.wikipedia.org/wiki/Leroy_Hood

    Leroy Hood won the 2011 Fritz J. and Dolores H. Russ Prize "for automating DNA sequencing that revolutionized biomedicine and forensic science"; [143] the 2011 National Medal of Science, presented at a White House ceremony by President Obama in early 2013; [144] the IEEE Medal for Innovations in Healthcare Technology in 2014, [9] and the 2016 ...

  4. List of sequence alignment software - Wikipedia

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

    Y. Totoki (based on O. Gotoh) 1991 and later: PSAlign Alignment preserving non-heuristic: Both: Local or global: S.H. Sze, Y. Lu, Q. Yang. 2006: RevTrans Combines DNA and Protein alignment, by back translating the protein alignment to DNA. DNA/Protein (special) Local or global: Wernersson and Pedersen: 2003 (newest version 2005) SAGA

  5. BRB-seq - Wikipedia

    en.wikipedia.org/wiki/BRB-seq

    A successful library contains fragments in the range of 300 – 1000 bp with a peak of 400-700 bp. Unlike standard bulk RNA-seq methods which require around 30 million reads per sample for robust gene expression information, for BRB-seq, a sequencing depth of between one and five million reads per sample is sufficient to detect the majority of ...

  6. Molecular Evolutionary Genetics Analysis - Wikipedia

    en.wikipedia.org/wiki/Molecular_Evolutionary...

    One of the challenges associated with evolutionary genetic analysis is the presence of ambiguous states such as R, Y, and T. These states often arise from sequence errors or incomplete datasets. However, MEGA offers several resources to handle ambiguous states, including the deletion of sites that have an ambiguity score higher than the Site ...

  7. 2 base encoding - Wikipedia

    en.wikipedia.org/wiki/2_Base_Encoding

    2 Base Encoding, also called SOLiD (sequencing by oligonucleotide ligation and detection), is a next-generation sequencing technology developed by Applied Biosystems and has been commercially available since 2008. These technologies generate hundreds of thousands of small sequence reads at one time.

  8. Transcriptomics technologies - Wikipedia

    en.wikipedia.org/wiki/Transcriptomics_technologies

    Sequencing technology platforms commonly used for RNA-Seq [77] [78] Platform Commercial release Typical read length Maximum throughput per run Single read accuracy RNA-Seq runs deposited in the NCBI SRA (Oct 2016) [79] 454 Life Sciences: 2005 700 bp 0.7 Gbp 99.9% 3548 Illumina: 2006 50–300 bp 900 Gbp 99.9% 362903 SOLiD: 2008 50 bp 320 Gbp 99. ...

  9. CITE-Seq - Wikipedia

    en.wikipedia.org/wiki/CITE-Seq

    CITE-Seq (Cellular Indexing of Transcriptomes and Epitopes by Sequencing) is a method for performing RNA sequencing along with gaining quantitative and qualitative information on surface proteins with available antibodies on a single cell level. [1]