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  2. Biopython - Wikipedia

    en.wikipedia.org/wiki/Biopython

    A core concept in Biopython is the biological sequence, and this is represented by the Seq class. [11] A Biopython Seq object is similar to a Python string in many respects: it supports the Python slice notation, can be concatenated with other sequences and is immutable. In addition, it includes sequence-specific methods and specifies the ...

  3. List of RNA-Seq bioinformatics tools - Wikipedia

    en.wikipedia.org/wiki/List_of_RNA-Seq...

    fastqp Simple FASTQ quality assessment using Python. Kraken: [9] A set of tools for quality control and analysis of high-throughput sequence data. HTSeq [10] The Python script htseq-qa takes a file with sequencing reads (either raw or aligned reads) and produces a PDF file with useful plots to assess the technical quality of a run.

  4. SPAdes (software) - Wikipedia

    en.wikipedia.org/wiki/SPAdes_(software)

    Assembly of single cell data is difficult due to non-uniform read coverage, variation in insert length, high levels of sequencing errors and chimeric reads. [ 8 ] [ 12 ] [ 13 ] Therefore, the new algorithmic approach, SPAdes, was designed to address these issues.

  5. Multiple sequence alignment - Wikipedia

    en.wikipedia.org/wiki/Multiple_sequence_alignment

    Multiple sequence alignment (MSA) is the process or the result of sequence alignment of three or more biological sequences, generally protein, DNA, or RNA. These alignments are used to infer evolutionary relationships via phylogenetic analysis and can highlight homologous features between sequences.

  6. Sequential pattern mining - Wikipedia

    en.wikipedia.org/wiki/Sequential_Pattern_Mining

    Sequential pattern mining is a topic of data mining concerned with finding statistically relevant patterns between data examples where the values are delivered in a sequence. [ 1 ] [ 2 ] It is usually presumed that the values are discrete, and thus time series mining is closely related, but usually considered a different activity.

  7. Open reading frame - Wikipedia

    en.wikipedia.org/wiki/Open_reading_frame

    The ORF Finder (Open Reading Frame Finder) [16] is a graphical analysis tool which finds all open reading frames of a selectable minimum size in a user's sequence or in a sequence already in the database. This tool identifies all open reading frames using the standard or alternative genetic codes.

  8. Seq2seq - Wikipedia

    en.wikipedia.org/wiki/Seq2seq

    Shannon's diagram of a general communications system, showing the process by which a message sent becomes the message received (possibly corrupted by noise). seq2seq is an approach to machine translation (or more generally, sequence transduction) with roots in information theory, where communication is understood as an encode-transmit-decode process, and machine translation can be studied as a ...

  9. Longest common subsequence - Wikipedia

    en.wikipedia.org/wiki/Longest_common_subsequence

    They match, so G is appended to the upper left sequence, LCS(R 0, C 1), which is (ε), giving (εG), which is (G). For LCS(R 1, C 3), G and C do not match. The sequence above is empty; the one to the left contains one element, G. Selecting the longest of these, LCS(R 1, C 3) is (G). The arrow points to the left, since that is the longest of the ...