[1]
Agostino, M.J. 2013. Practical bioinformatics. Garland Science.
[2]
Allison et al., D.B. 2006. ‘Microarray data analysis: from disarray to consolidation and consensus’. Nature Reviews Genetics. 7, 1 (2006), 55–65.
[3]
Aritua et al., V. 2015. ‘The draft genome sequence of Xanthomonas species strain Nyagatare, isolated from diseased bean in Rwanda’. FEMS Microbiology Letters. 362, 4 (2015), 1–4.
[4]
Armstrong, L. 2013. Chapter 1: ‘Introduction to the Study of Epigenetics’. Epigenetics. Garland Science. 1–5.
[5]
Armstrong, L. 2013. Epigenetics. Garland Science.
[6]
Biosciences - LibGuides at University of Exeter: http://libguides.exeter.ac.uk.
[7]
Brown, T.A. 2017. Chapter 4: ‘Genome Sequencing’. Genomes 4. Garland Science. 87–117.
[8]
Brown, T.A. 2017. Genomes 4. Garland Science.
[9]
Clyde, D. 2018. ‘The girl with Neanderthal and Denisovan parents’. Nature Reviews Genetics. 19, 11 (2018), 668–669.
[10]
Eddy, S.R. 2004. ‘What is a hidden Markov model?’ Nature Biotechnology. 22, 10 (2004), 1315–1316.
[11]
Eyre et al., D.W. 2018. ‘A Candida auris Outbreak and Its Control in an Intensive Care Setting’. New England Journal of Medicine. 379, 14 (2018), 1322–1331.
[12]
Jobling, M.A. et al. 2013. Human Evolutionary Genetics: Origins, Peoples and Disease. Garland Science.
[13]
Learn.Genetics 2018. The Epigenome at a Glance. University of Utah.
[14]
Lesk, A.M. 2017. Chapter 1: ‘Introduction and Background’. Introduction to Genomics. Oxford University Press. 1–61.
[15]
Lesk, A.M. 2014. Introduction to bioinformatics. Oxford University Press.
[16]
Lesk, A.M. 2017. Introduction to Genomics. Oxford University Press.
[17]
Lesk, A.M. 2012. Introduction to Genomics. Oxford University Press.
[18]
Lesk, A.M. 2017. Introduction to Genomics. Oxford University Press.
[19]
Lesk, A.M. 2012. Introduction to Genomics. Oxford University Press.
[20]
Lesk, A.M. 2017. Introduction to Genomics. Oxford University Press.
[21]
Lesk, A.M. 2012. Introduction to Genomics. Oxford University Press.
[22]
Lesk, A.M. 2017. Introduction to Genomics. Oxford University Press.
[23]
Lesk, A.M. 2012. Introduction to Genomics. Oxford University Press.
[24]
Lesk, A.M. 2017. Introduction to Genomics. Oxford University Press.
[25]
Lesk, A.M. 2012. Introduction to Genomics. Oxford University Press.
[26]
Lesk, A.M. 2017. Introduction to Genomics. Oxford University Press.
[27]
Lesk, A.M. 2012. Introduction to Genomics. Oxford University Press.
[28]
Lesk, A.M. 2017. Introduction to Genomics. Oxford University Press.
[29]
Lesk, A.M. 2012. Introduction to Genomics. Oxford University Press.
[30]
Lesk, A.M. 2017. Introduction to Genomics. Oxford University Press.
[31]
Lesk, A.M. 2012. Introduction to Genomics. Oxford University Press.
[32]
Lesk, A.M. 2017. Introduction to Genomics. Oxford University Press.
[33]
Lesk, A.M. 2012. Introduction to Genomics. Oxford University Press.
[34]
Lesk, A.M. 2017. Introduction to Genomics. Oxford University Press.
[35]
Lesk, A.M. 2012. Introduction to Genomics. Oxford University Press.
[36]
Lesk, A.M. 2017. Introduction to Genomics. Oxford University Press.
[37]
Lesk, A.M. 2012. Introduction to Genomics. Oxford University Press.
[38]
Morcrette et al., H. 2018. ‘Genome Sequence of Staphylococcus aureus Ex1, Isolated from a Patient with Spinal Osteomyelitis’ [in] Genome Announcements. Genome Announcements. 6, 26 (2018).
[39]
Nagarajan, N. and Pop, M. 2013. ‘Sequence assembly demystified’. Nature Reviews Genetics. 14, 3 (2013), 157–167.
[40]
Rasmussen et al., M. 2010. ‘Ancient human genome sequence of an extinct Palaeo-Eskimo’. Nature. 463, 7282 (2010), 757–762.
[41]
Satta, G. et al. 2017. ‘Mycobacterium tuberculosis and whole genome sequencing: a practical guide and online tools available for the clinical microbiologist’. Clinical Microbiology and Infection. 23, 2 (2017), 69–72.
[42]
Sjölander et al., K. 1996. ‘Dirichlet mixtures: a method for improved detection of weak but significant protein sequence homology’. Bioinformatics. 12, 4 (1996), 327–345.
[43]
Snyder, M. 2015. Genomics and Personalized Medicine: What Everyone Needs to Know.
[44]
Strachan, T. et al. 2015. Genetics and Genomics in Medicine. Garland Science.
[45]
Studholme, D.J. 2016. ‘Genome Update. Let the consumer beware: Streptomyces genome sequence quality’. Microbial Biotechnology. 9, 1 (2016), 3–7.
[46]
Wang, Z. et al. 2009. ‘RNA-Seq: a revolutionary tool for transcriptomics’. Nature Reviews Genetics. 10, 1 (2009), 57–63.
[47]
Warren, M. 2018. ‘Mum’s a Neanderthal, Dad’s a Denisovan: First discovery of an ancient-human hybrid’. Nature. 560, 7719 (2018), 417–418.
[48]
Weyrich et al., L.S. 2017. ‘Neanderthal behaviour, diet, and disease inferred from ancient DNA in dental calculus’. Nature. 544, 7650 (2017), 357–361.