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  2. De novo peptide sequencing - Wikipedia

    en.wikipedia.org/wiki/De_novo_peptide_sequencing

    For example, mass differences between a n and a n-1, b n and b n-1, c n and c n-1 are the same. Identify y n-1-ion at the high-mass end of the spectrum. 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.

  3. SNP array - Wikipedia

    en.wikipedia.org/wiki/SNP_array

    For example, genome-wide association studies have identified SNPs associated with diseases such as rheumatoid arthritis [8] and prostate cancer. [9] A SNP array can also be used to generate a virtual karyotype using software to determine the copy number of each SNP on the array and then align the SNPs in chromosomal order.

  4. Sanger sequencing - Wikipedia

    en.wikipedia.org/wiki/Sanger_sequencing

    Common challenges of DNA sequencing with the Sanger method include poor quality in the first 15–40 bases of the sequence due to primer binding and deteriorating quality of sequencing traces after 700–900 bases. Base calling software such as Phred typically provides an estimate of quality to aid in trimming of low-quality regions of sequences.

  5. Shotgun proteomics - Wikipedia

    en.wikipedia.org/wiki/Shotgun_proteomics

    One example of this is a study by Washburn, Wolters, and Yates in which they used shotgun proteomics on the proteome of a Saccharomyces cerevisiae strain grown to mid-log phase. They were able to detect and identify 1,484 proteins as well as identify proteins rarely seen in proteome analysis, including low-abundance proteins like transcription ...

  6. Sequence assembly - Wikipedia

    en.wikipedia.org/wiki/Sequence_assembly

    The complexity of sequence assembly is driven by two major factors: the number of fragments and their lengths. While more and longer fragments allow better identification of sequence overlaps, they also pose problems as the underlying algorithms show quadratic or even exponential complexity behaviour to both number of fragments and their length.

  7. DNA sequencing theory - Wikipedia

    en.wikipedia.org/wiki/DNA_sequencing_theory

    DNA sequencing theory is the broad body of work that attempts to lay analytical foundations for determining the order of specific nucleotides in a sequence of DNA, otherwise known as DNA sequencing. The practical aspects revolve around designing and optimizing sequencing projects (known as "strategic genomics"), predicting project performance ...

  8. Shortest common supersequence - Wikipedia

    en.wikipedia.org/wiki/Shortest_common_supersequence

    In the SCS problem, two sequences X and Y are given, and the task is to find a shortest possible common supersequence of these sequences. In general, an SCS is not unique. For two input sequences, an SCS can be formed from a longest common subsequence (LCS) easily. For example, the longest common subsequence of X [] = and Y [] = is Z [] =.

  9. Larry French column: Three 'young' seniors top 700 to ...

    www.aol.com/larry-french-column-three-young...

    Bruce Stanton, John Stermer and Tim DeGraw all topped the 700 mark at Crystal Lanes in Corning. See the latest scores. Larry French column: Three 'young' seniors top 700 to highlight latest ...