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001 oapen86217
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006 m o d
007 cr|mn|---annan
008 231218s2022 xx |||||o ||| 0|eng d
020 _a9780367903718
020 _a9781003247432
020 _a9781003247432
020 _a9781032161907
024 7 _a10.1201/9781003247432
_2doi
040 _aoapen
_coapen
041 0 _aeng
042 _adc
100 1 _aRogers, Scott
_4edt
245 1 0 _aMolecular Analyses
260 _bTaylor & Francis
_c2022
300 _a1 online resource
336 _atext
_btxt
_2rdacontent
337 _acomputer
_bc
_2rdamedia
338 _aonline resource
_bcr
_2rdacarrier
506 0 _aFree-to-read
_fUnrestricted online access
_2star
520 _aDNA and RNA extraction methods from a variety of tissues and samples are now routine, including extraction from single cells. Many methods are now automated. Sequencing efficiency has reached the point where it is now possible to obtain gigabases of data, both quickly and inexpensively. Such methods permit the identification of gene versions, including those associated with disease (e.g. small nucleotide polymorphism analyses, or SNPs). The general public as well as clinicians can now access a wide variety of literature on the molecular bases of diseases, allowing them to better assess disease risks and treatments. This volume concentrates on medically-focused methods, and therefore the major audience will be medical professionals, students, and those involved in medically-related research endeavors. There are also papers in this volume dealing specifically with methods developed to analyze large sequence data sets. Many methods reviewed herein are more broadly applicable to other fields in biology, chemistry, bioinformatics, and bioengineering, and are intended for a broad readership
540 _aAll rights reserved
_uhttp://oapen.org/content/about-rights
546 _aEnglish
653 _aGene Sequences, Next Generation sequencing, Nucleotide, Phylogenomics
700 1 _aRogers, Scott
_4oth
793 0 _aOAPEN Library.
856 4 0 _uhttps://library.oapen.org/handle/20.500.12657/86217
_70
_zFree-to-read: OAPEN Library: description of the publication
999 _c36875
_d36875