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  2. List of sequence alignment software - Wikipedia

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

    Version 0.2 of October 2016, supports the algorithms BWA-MEM, BWA-backtrack, and BWA-ALN. All of them work with single-reads and paired-end reads. Yes Low quality bases trimming Yes Yes Free, GPL 3 [57] 2016 SSAHA, SSAHA2 Fast for a small number of variants Proprietary, freeware for academic and noncommercial use Stampy For Illumina reads.

  3. Scaffolding (bioinformatics) - Wikipedia

    en.wikipedia.org/wiki/Scaffolding_(bioinformatics)

    Although Illumina platforms are now able to generate mate pair reads with average lengths of 150bp, they were originally only able to generate reads of 75bp or less, which caused many people in the science community to doubt a reliable reference genome could ever be constructed with short read technology. The increased difficulty of contig and ...

  4. Coverage (genetics) - Wikipedia

    en.wikipedia.org/wiki/Coverage_(genetics)

    Sequence coverage (or depth) is the number of unique reads that include a given nucleotide in the reconstructed sequence. [1] [2] Deep sequencing refers to the general concept of aiming for high number of unique reads of each region of a sequence. [3] Physical coverage, the cumulative length of reads or read pairs expressed as a multiple of ...

  5. SAM (file format) - Wikipedia

    en.wikipedia.org/wiki/SAM_(file_format)

    Description (Paired Read Interpretation) 1 000000000001: template having multiple templates in sequencing (read is paired) 2 000000000010: each segment properly aligned according to the aligner (read mapped in proper pair) 4 000000000100: segment unmapped (read1 unmapped) 8 000000001000: next segment in the template unmapped (read2 unmapped) 16

  6. Read (biology) - Wikipedia

    en.wikipedia.org/wiki/Read_(biology)

    Sequencing technologies vary in the length of reads produced. Reads of length 20-40 base pairs (bp) are referred to as ultra-short. [2] Typical sequencers produce read lengths in the range of 100-500 bp. [3] However, Pacific Biosciences platforms produce read lengths of approximately 1500 bp. [4] Read length is a factor which can affect the results of biological studies. [5]

  7. Ohio Man Allegedly Slammed Infant Who Wouldn’t Stop ... - AOL

    www.aol.com/ohio-man-allegedly-slammed-infant...

    An Ohio man allegedly slammed a 15-month-old girl on the floor after she wouldn’t stop crying, fracturing her skull. Two weeks later, she died of her injuries.

  8. De novo sequence assemblers - Wikipedia

    en.wikipedia.org/wiki/De_novo_sequence_assemblers

    These algorithms typically do not work well for larger read sets, as they do not easily reach a global optimum in the assembly, and do not perform well on read sets that contain repeat regions. [1] Early de novo sequence assemblers, such as SEQAID [ 2 ] (1984) and CAP [ 3 ] (1992), used greedy algorithms, such as overlap-layout-consensus (OLC ...

  9. 30 Color Photos Photographers Took 100 Years Ago That Still ...

    www.aol.com/44-old-color-photos-showing...

    Image credits: Photoglob Zürich As evident from Niépce's and Maxwell's experiments, and as photographic process historian Mark Osterman told Bored Panda, the processes behind colored photographs ...