Comparing bioinformatic pipelines for microbial 16S rRNA amplicon sequencing von Prodan, Andrei, Tremaroli, Valentina, Brolin, Harald, Zwinderman, Aeilko H, Nieuwdorp, Max, Levin, Evgeni

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An extensive evaluation of read trimming effects on Illumina NGS data analysis von Del Fabbro, Cristian, Scalabrin, Simone, Morgante, Michele, Giorgi, Federico M

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Genetic risk scores and dementia risk across different ethnic groups in UK Biobank von Mukadam, Naaheed, Giannakopoulou, Olga, Bass, Nick, Kuchenbaecker, Karoline, McQuillin, Andrew

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Signal-based optical map alignment von Akdel, Mehmet, van de Geest, Henri, Schijlen, Elio, van Rijswijck, Irma M. H, Smid, Eddy J, Sanchez-Perez, Gabino, de Ridder, Dick

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DNA isolation protocol effects on nuclear DNA analysis by microarrays, droplet digital PCR, and whole genome sequencing, and on mitochondrial DNA copy number estimation von Nacheva, Elizabeth, Mokretar, Katya, Soenmez, Aynur, Pittman, Alan M, Grace, Colin, Valli, Roberto, Ejaz, Ayesha, Vattathil, Selina, Maserati, Emanuela, Houlden, Henry, Taanman, Jan-Willem, Schapira, Anthony H, Proukakis, Christos

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Empirical validation of pooled whole genome population re-sequencing in Drosophila melanogaster von Zhu, Yuan, Bergland, Alan O, González, Josefa, Petrov, Dmitri A

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C3-PRO: Connecting ResearchKit to the Health System Using i2b2 and FHIR von Pfiffner, Pascal B, Pinyol, Isaac, Natter, Marc D, Mandl, Kenneth D

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Limitations of the human reference genome for personalized genomics von Rosenfeld, Jeffrey A, Mason, Christopher E, Smith, Todd M

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Amplicon sequencing of colorectal cancer: variant calling in frozen and formalin-fixed samples von Betge, Johannes, Kerr, Grainne, Miersch, Thilo, Leible, Svenja, Erdmann, Gerrit, Galata, Christian L, Zhan, Tianzuo, Gaiser, Timo, Post, Stefan, Ebert, Matthias P, Horisberger, Karoline, Boutros, Michael

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Rare gene deletions in genetic generalized and Rolandic epilepsies von Jabbari, Kamel, Bobbili, Dheeraj R, Lal, Dennis, Reinthaler, Eva M, Schubert, Julian, Wolking, Stefan, Sinha, Vishal, Motameny, Susanne, Thiele, Holger, Kawalia, Amit, Altmüller, Janine, Toliat, Mohammad Reza, Kraaij, Robert, van Rooij, Jeroen, Uitterlinden, André G, Ikram, M Arfan, Zara, Federico, Lehesjoki, Anna-Elina, Krause, Roland, Zimprich, Fritz, Sander, Thomas, Neubauer, Bernd A, May, Patrick, Lerche, Holger, Nürnberg, Peter

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BOOGIE: Predicting Blood Groups from High Throughput Sequencing Data von Giollo, Manuel, Minervini, Giovanni, Scalzotto, Marta, Leonardi, Emanuela, Ferrari, Carlo, Tosatto, Silvio C E

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Importance of human leukocyte antigen (HLA) class I and II alleles on the risk of multiple sclerosis von Link, Jenny, Kockum, Ingrid, Lorentzen, Aslaug R, Lie, Benedicte A, Celius, Elisabeth G, Westerlind, Helga, Schaffer, Marie, Alfredsson, Lars, Olsson, Tomas, Brynedal, Boel, Harbo, Hanne F, Hillert, Jan

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Characterisation of genetic variation in ST8SIA2 and its interaction region in NCAM1 in patients with bipolar disorder von Shaw, Alex D, Tiwari, Yash, Kaplan, Warren, Heath, Anna, Mitchell, Philip B, Schofield, Peter R, Fullerton, Janice M

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Assessing the impact of copy number variants on miRNA genes in autism by Monte Carlo simulation von Marrale, Maurizio, Albanese, Nadia Ninfa, Calì, Francesco, Romano, Valentino

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Copy number variation in Thai population von Suktitipat, Bhoom, Naktang, Chaiwat, Mhuantong, Wuttichai, Tularak, Thitima, Artiwet, Paramita, Pasomsap, Ekawat, Jongjaroenprasert, Wallaya, Fuchareon, Suthat, Mahasirimongkol, Surakameth, Chantratita, Wasan, Yimwadsana, Boonsit, Charoensawan, Varodom, Jinawath, Natini

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RAMBO-K: Rapid and Sensitive Removal of Background Sequences from Next Generation Sequencing Data von Tausch, Simon H, Renard, Bernhard Y, Nitsche, Andreas, Dabrowski, Piotr Wojciech

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Capric acid inhibits NO production and STAT3 activation during LPS-induced osteoclastogenesis von Park, Eun-Jung, Kim, Sun A, Choi, Yong-Min, Kwon, Hyuk-Kwon, Shim, Wooyoung, Lee, Gwang, Choi, Sangdun

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Determination of a Screening Metric for High Diversity DNA Libraries von Guido, Nicholas J, Handerson, Steven, Joseph, Elaine M, Leake, Devin, Kung, Li A

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Haplotype phasing and inheritance of copy number variants in nuclear families von Palta, Priit, Kaplinski, Lauris, Nagirnaja, Liina, Veidenberg, Andres, Möls, Märt, Nelis, Mari, Esko, Tõnu, Metspalu, Andres, Laan, Maris, Remm, Maido

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Analysis of microsatellite variation in Drosophila melanogaster with population-scale genome sequencing von Fondon, 3rd, John W, Martin, Andy, Richards, Stephen, Gibbs, Richard A, Mittelman, David

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