Abstract
By tracking pathogen outbreaks using whole genome sequencing, medical microbiology is currently being transformed into genomic epidemiology. This change in technology is leading to the rapid accumulation of large samples of closely related genome sequences. Summarizing such samples into phylogenies can be computationally challenging. Our program andi quickly computes accurate pairwise distances between up to thousands of bacterial genomes. Working under the UNIX command line, we show how andi can be used to transform genomes to phylogenies with support values ready to be printed or integrated into documents.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
References
Allard MW, Strain E, Melka D, Bunning K, Musser SM, Brown EW, Timme R (2016) Practical value of food pathogen traceability through building a whole-genome sequencing network and database. J Clin Microbiol 54:1975–1983
Cherry JL (2017) A practical exact maximum compatibility algorithm for reconstruction of recent evolutionary history. BMC Bioinf 18:127
Criscuolo A, Gascuel O (2008) Fast NJ-like algorithms to deal with incomplete distance matrices. BMC Bioinf 9:166
Didelot X, Bowden R, Wilson DJ, Peto TEA, Crook DW (2012) Transforming clinical microbiology with bacterial genome sequencing. Nat Rev Genet 13:601–612
Felsenstein J (1985) Confidence limits on phylogenies: an approach using the bootstrap. Evolution 39:783–791
Felsenstein J (2004) Inferring phylogenies. Sinauer, Sunderland
Felsenstein J (2005) PHYLIP (phylogeny interference package) version 3.6
Haubold B (2014) Alignment-free phylogenetics and population genetics. Brief Bioinf 15:407–418
Haubold B, Pfaffelhuber P, Domazet-Lošo M, Wiehe T (2009) Estimating mutation distances from unaligned genomes. J Comput Biol 16:1487–1500
Haubold B, Klötzl F, Pfaffelhuber P (2015) andi: fast and accurate estimation of evolutionary distances between closely related genomes. Bioinformatics 31:1169–75
Hudson RR (2002) Generating samples under a Wright–Fisher neutral model of genetic variation. Bioinformatics 18:337–338
Jukes TH, Cantor CR (1969) Evolution of protein molecules. In: Munro HN (ed) Mammalian protein metabolism, vol 3, Academic Press, New York, pp 21–132
Klötzl F, Haubold B (2016) Support values for genome phylogenies. Life 6:11
Langmead B, Trapnell C, Pop M, Salzberg SL (2009) Ultrafast and memory-efficient alignment of short DNA sequences to the human genome. Genome Biol 10:R25
Li H, Durbin R (2009) Fast and accurate short read alignment with Burrows–Wheeler transform. Bioinformatics 25:1754–1760
Manber U, Myers EW (1993) Suffix arrays: a new method for on-line string searches. SIAM J Comput 22:935–948
Ohlebusch E (2013) Bioinformatics algorithms: sequence analysis, genome rearrangements, and phylogenetic reconstruction. Enno Ohlebusch, Ulm
Rasko D, Webster D, Sahl J, Bashir A, Boisen N, Scheutz F, Paxinos E, Sebra R, Chin C, Iliopoulos D, Klammer A, Peluso P, Lee L, Kislyuk A, Bullard J, Kasarskis A, Wang S, Eid J, Rank D, Redman J, Steyert S, Frimodt-Moller J, Struve C, Petersen A, Krogfelt K, Nataro J, Schadt E, Waldor M (2011) Origins of the E. coli strain causing an outbreak of hemolytic-uremic syndrome in Germany. N Engl J Med 365:709–717. https://doi.org/10.1056/NEJMoa1106920
Smith TF, Waterman MS (1981) Identification of common molecular subsequences. J Mol Biol 147:195–197
Swofford DL, Olsen GJ, Waddell PJ, Hillis DM (1996) Phylogenetic inference. In: Hillis DM, Craig M, Marble BK (eds) Molecular systematics, 2nd edn, Sinauer, Sunderland, pp 407–514
Tang P, Croxen MA, Hasan MR, Hsiao WWL, Hoang LM (2017) Infection control in the new age of genomic epidemiology. Am J Infect Control 45:170–179
Zielezinski A, Girgis HZ, Bernard G, Leimeister CA, Tang K, Dencker T, Lau AK, Röhling S, Choi J, Waterman MS, Comin M, Kim SH, Vinga S, Almeida JS, Chan CX, James BT, Sun F, Morgenstern B, Karlowski WM (2019) Benchmarking of alignment-free sequence comparison methods. Genome Biol 20:140. https://doi.org/10.1101/611137. https://www.biorxiv.org/content/early/2019/04/16/611137. https://www.biorxiv.org/content/early/2019/04/16/611137.full.pdf
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2021 Springer Science+Business Media, LLC, part of Springer Nature
About this protocol
Cite this protocol
Haubold, B., Klötzl, F. (2021). Fast Phylogeny Reconstruction from Genomes of Closely Related Microbes. In: Mengoni, A., Bacci, G., Fondi, M. (eds) Bacterial Pangenomics. Methods in Molecular Biology, vol 2242. Humana, New York, NY. https://doi.org/10.1007/978-1-0716-1099-2_6
Download citation
DOI: https://doi.org/10.1007/978-1-0716-1099-2_6
Published:
Publisher Name: Humana, New York, NY
Print ISBN: 978-1-0716-1098-5
Online ISBN: 978-1-0716-1099-2
eBook Packages: Springer Protocols