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Ligation Bias in Illumina Next-Generation DNA Libraries: Implications for Sequencing Ancient Genomes
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Mappers can show different performance depending on the experimental procedure followed during sample preparation, such as the type of DNA library constructed and whether or not extracts were USER-treated.
“Mappers can show different performance depending on the experimental procedure followed during sample preparation, such as the type of DNA library constructed 185 and whether or not extracts were USER-treated 184 .”
From Ancient DNA analysis (2021) · cites this paper as [185]
The Conclusion (page unavailable) says library-preparation methods bias read composition and, together with variation in mappability, affect genomic coverage. The Sequence analysis methods (page unavailable) describe using BWA, but the paper does not compare mappers or show that their performance changes with library type. The separate USER-treatment citation is not assessed here. (LLM, conf=0.85)
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Genetic history of an archaic hominin group from Denisova Cave in Siberia
Reich, D., Green, R. E., Kircher, M., Krause, J., Patterson, N., Durand, E. Y., Viola, B., Briggs, A. W., Stenzel, U., Johnson, P. L. F., et al. (2010) · Nature · doi:10.1038/nature09710 · Cited by 1,991
A high-coverage genome sequence from an archaic denisovan individual
Meyer, M., Kircher, M., Gansauge, M.-T., Li, H., Racimo, F., Mallick, S., Schraiber, J. G., Jay, F., Prüfer, K., de Filippo, C., et al. (2012) · Science · doi:10.1126/science.1224344 · Cited by 1,967
mapDamage2.0: fast approximate Bayesian estimates of ancient DNA damage parameters
Jónsson, H., Ginolhac, A., Schubert, M., Johnson, P. L. F., & Orlando, L. (2013) · Bioinformatics · doi:10.1093/bioinformatics/btt193 · Cited by 1,669
Self-citationAncient human genome sequence of an extinct Palaeo-Eskimo
Rasmussen, M., Li, Y., Lindgreen, S., Pedersen, J. S., Albrechtsen, A., Moltke, I., Metspalu, M., Metspalu, E., Kivisild, T., Gupta, R., et al. (2010) · Nature · doi:10.1038/nature08835 · Cited by 849
Self-citationAn aboriginal Australian genome reveals separate human dispersals into Asia
Rasmussen, M., Guo, X., Wang, Y., Lohmueller, K. E., Rasmussen, S., Albrechtsen, A., Skotte, L., Lindgreen, S., Metspalu, M., Jombart, T., et al. (2011) · Science · doi:10.1126/science.1211177 · Cited by 787
Self-citationBiases in Illumina transcriptome sequencing caused by random hexamer priming
Hansen, K. D., Brenner, S. E., & Dudoit, S. (2010) · Nucleic Acids Research · doi:10.1093/nar/gkq224 · Cited by 713
Hofreiter, M. (2001) · Nucleic Acids Research · doi:10.1093/nar/29.23.4793 · Cited by 684
Temporal patterns of nucleotide misincorporations and DNA fragmentation in ancient DNA
Sawyer, S., Krause, J., Guschanski, K., Savolainen, V., & Pääbo, S. (2012) · PLoS ONE · doi:10.1371/journal.pone.0034131 · Cited by 489
New insights into the Tyrolean Iceman's origin and phenotype as inferred by whole-genome sequencing
Keller, A., Graefen, A., Ball, M., Matzas, M., Boisguerin, V., Maixner, F., Leidinger, P., Backes, C., Khairat, R., Forster, M., et al. (2012) · Nature Communications · doi:10.1038/ncomms1701 · Cited by 437
mapDamage: testing for damage patterns in ancient DNA sequences
Ginolhac, A., Rasmussen, M., Gilbert, M. T. P., Willerslev, E., & Orlando, L. (2011) · Bioinformatics · doi:10.1093/bioinformatics/btr347 · Cited by 363
Self-citationImproving ancient DNA read mapping against modern reference genomes
Schubert, M., Ginolhac, A., Lindgreen, S., Thompson, J. F., AL-Rasheid, K. A., Willerslev, E., Krogh, A., & Orlando, L. (2012) · BMC Genomics · doi:10.1186/1471-2164-13-178 · Cited by 325
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Flagged first, then by citations
Research works printed but not linked: 39
- RE Green, 2010, A draft sequence of the Neandertal genome, Science, 328, 710, 10.1126/science.1188021 · DOI · Paper page
- D Serre, 2004, No evidence of Neandertal mtDNA contribution to early modern humans, PLoS Biology, 2, E57, 10.1371/journal.pbio.0020057 · DOI
- HN Poinar, 2006, Metagenomics to paleogenomics: large-scale sequencing of mammoth DNA, Science, 311, 392, 10.1126/science.1123360 · DOI
- HA Burbano, 2010, Targeted investigation of the Neandertal genome by array-based sequence capture, Science, 328, 723, 10.1126/science.1188046 · DOI
- P Skoglund, 2012, Origins and genetic legacy of Neolithic farmers and hunter-gatherers in Europe, Science, 336, 466, 10.1126/science.1216304 · DOI · Paper page
- W Miller, 2008, Sequencing the nuclear genome of the extinct woolly mammoth, Nature, 456, 387, 10.1038/nature07446 · DOI
- JP Noonan, 2005, Genomic sequencing of Pleistocene cave bears, Science, 309, 597, 10.1126/science.1113485 · DOI
- J Krause, 2008, Mitochondrial genomes reveal an explosive radiation of extinct and extant bears near the Miocene-Pliocene boundary, BMC Evol Biol, 8, 220, 10.1186/1471-2148-8-220 · DOI
- ML Metzker, 2010, Sequencing technologies – the next generation, Nat Rev Genet, 11, 31, 10.1038/nrg2626 · DOI · Paper page
- AW Briggs, 2007, Patterns of damage in genomic DNA sequences from a Neandertal, Proc Natl Acad Sci U S A, 104, 14616, 10.1073/pnas.0704665104 · DOI · Paper page
- A Hansen, 2001, Statistical evidence for miscoding lesions in ancient DNA templates, Mol Biol Evol, 18, 262, 10.1093/oxfordjournals.molbev.a003800 · DOI
- Meyer M, Kircher M (2010) Illumina sequencing library preparation for highly multiplexed target capture and sequencing. Cold Spring Harb Protoc <comment>doi:10.1101</comment> · DOI
- J Krause, 2010, The complete mitochondrial DNA genome of an unknown hominin from southern Siberia, Nature, 464, 894, 10.1038/nature08976 · DOI
- L Orlando, 2011, True single-molecule DNA sequencing of a pleistocene horse bone, Genome Res, 21, 1705, 10.1101/gr.122747.111 · DOI
- AW Briggs, 2012, Preparation of next-generation sequencing libraries from damaged DNA, Methods Mol Biol, 840, 143, 10.1007/978-1-61779-516-9_18 · DOI
- A Ginolhac, 2012, Improving the performance of true single molecule sequencing for ancient DNA, BMC Genomics, 13, 177, 10.1186/1471-2164-13-177 · DOI
- M García-Garcerà, 2011, Fragmentation of Contaminant and Endogenous DNA in Ancient Samples Determined by Shotgun Sequencing; Prospects for Human Palaeogenomics, PLoS One, 6, e24161, 10.1371/journal.pone.0024161 · DOI
- AW Briggs, 2010, Removal of deaminated cytosines and detection of in vivo methylation in ancient DNA, Nucleic Acids Res, 38, e87, 10.1093/nar/gkp1163 · DOI · Paper page
- MA Quail, 2008, A large genome center's improvements to the Illumina sequencing system, Nat Methods, 5, 1005, 10.1038/nmeth.1270 · DOI
- ME Allentoft, 2012, The half-life of DNA in bone: measuring decay kinetics in 158 dated fossils, Proc Biol Sci, 279, 4724, 10.1098/rspb.2012.1745 · DOI · Paper page
- JT Vilstrup, 2013, Mitochondrial Phylogenomics of Modern and Ancient Equids, PLoS One, 8, e55950, 10.1371/journal.pone.0055950 · DOI
- N Rohland, 2007, Ancient DNA extraction from bones and teeth, Nature Protocols, 2, 1756, 10.1038/nprot.2007.247 · DOI
- L Orlando, 2009, Revising the recent evolutionary history of equids using ancient DNA, Proc Natl Acad Sci U S A, 106, 21754, 10.1073/pnas.0903672106 · DOI
- H Li, 2009, Fast and accurate short read alignment with Burrows-Wheeler transform, Bioinformatics, 25, 1754, 10.1093/bioinformatics/btp324 · DOI · Paper page
- S Lindgreen, 2012, AdapterRemoval: easy cleaning of next-generation sequencing reads, BMC Res Notes, 5, 337, 10.1186/1756-0500-5-337 · DOI
- Y Benjamini, 2012, Summarizing and correcting the GC content bias in high-throughput sequencing, Nucleic Acids Res, 40, e72, 10.1093/nar/gks001 · DOI · Paper page
- R Higuchi, 1984, DNA sequences from the quagga, an extinct member of the horse family, Nature, 312, 282, 10.1038/312282a0 · DOI
- L Orlando, 2003, Morphological convergence in Hippidion and Equus (Amerhippus) South American equids elucidated by ancient DNA analysis, J Mol Evol, 57, S29, 10.1007/s00239-003-0005-4 · DOI
- KI Bos, 2011, A draft genome of Yersinia pestis from victims of the Black Death, Nature, 478, 506, 10.1038/nature10549 · DOI · Paper page
- D Peters, 2011, Noninvasive prenatal diagnosis of a fetal microdeletion syndrome., N Engl J Med, 365, 1847, 10.1056/NEJMc1106975 · DOI
- J Wang, 2012, Genome-wide single-cell analysis of recombination activity and de novo mutation rates in human sperm, Cell, 150, 402, 10.1016/j.cell.2012.06.030 · DOI
- J Dabney, 2012, Length and GC-biases during sequencing library amplification: A comparison of various polymerase-buffer systems with ancient and modern DNA sequencing libraries, BioTechniques, 52, 87, 10.2144/000113809 · DOI · Paper page
- Kircher M, Stenzel U, Kelso J (2009) Improved base calling for the Illumina Genome Analyzer using machine learning strategies. Genome Biol <comment>doi:10.1186/gb-2009-10-8-r83</comment> · DOI
- Kircher M, Heyn P, Kelso J (2011) Addressing challenges in the production and analysis of illumina sequencing data. BMC Genomics <comment>doi:10.1186/1471-2164-12-382</comment> · DOI
- C Bon, 2012, Coprolites as a source of information on the genome and diet of the cave hyena., Proc Biol Sci, 279, 2825, 10.1098/rspb.2012.0358 · DOI
- CL Oskam, 2010, Fossil avian eggshell preserves ancient DNA., Proc Biol Sci, 277, 1991, 10.1098/rspb.2009.2019 · DOI
- S Overballe-Petersen, 2012, Next-generation sequencing offers new insights into DNA degradation, Trends Biotechnology, 30, 364, 10.1016/j.tibtech.2012.03.007 · DOI
- D Mitchell, 2005, Damage and repair of ancient DNA, Mutat Res, 571, 265, 10.1016/j.mrfmmm.2004.06.060 · DOI
- VJ Schuenemann, 2011, Targeted enrichment of ancient pathogens yielding the pPCP1 plasmid of Yersinia pestis from victims of the Black Death, Proc Natl Acad Sci U S A, 108, E746, 10.1073/pnas.1105107108 · DOI
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Orlando, L., Allaby, R., Skoglund, P., Der Sarkissian, C., Stockhammer, P. W., Ávila-Arcos, M. C., Fu, Q., Krause, J., Willerslev, E., Stone, A. C., et al. (2021) · Nature Reviews Methods Primers · doi:10.1038/s43586-020-00011-0 · Cited by 411
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Schubert, M., Jónsson, H., Chang, D., Der Sarkissian, C., Ermini, L., Ginolhac, A., Albrechtsen, A., Dupanloup, I., Foucal, A., Petersen, B., et al. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1416991111 · Cited by 324
Self-citationGenomic structure in Europeans dating back at least 36,200 years
Seguin-Orlando, A., Korneliussen, T. S., Sikora, M., Malaspinas, A.-S., Manica, A., Moltke, I., Albrechtsen, A., Ko, A., Margaryan, A., Moiseyev, V., et al. (2014) · Science · doi:10.1126/science.aaa0114 · Cited by 315
Self-citationHuman evolution: a tale from ancient genomes
Llamas, B., Willerslev, E., & Orlando, L. (2017) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2015.0484 · Cited by 100
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Metadata
- Authors
- Seguin-Orlando, A., Schubert, M., Clary, J., Stagegaard, J., Alberdi, M. T., Prado, J. L., Prieto, A., Willerslev, E., & Orlando, L.
- Venue
- PLoS ONE
- Publisher
- Public Library of Science (PLoS)
- Published
- 2013-10-29
- Volume
- 8
- Issue
- 10
- Pages
- e78575
- ISSN
- 1932-6203
- PMC
- PMC3812280
- Cited by
- 76
- References
- 11
- Language
- en
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