Technical Validation of a Hepatitis C Virus Whole Genome Sequencing Assay for Detection of Genotype and Antiviral Resistance in the Clinical Pathway von Manso, Carmen F, Bibby, David F, Lythgow, Kieren, Mohamed, Hodan, Myers, Richard, Williams, David, Piorkowska, Renata, Chan, Yuen T, Bowden, Rory, Ansari, M Azim, Ip, Camilla L C, Barnes, Eleanor, Bradshaw, Daniel, Mbisa, Jean L

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Clinical evaluation of a Hepatitis C Virus whole-genome sequencing pipeline for genotyping and resistance testing von Bradshaw, Daniel, Bibby, David F., Manso, Carmen F., Piorkowska, Renata, Mohamed, Hodan, Ledesma, Juan, Bubba, Laura, Chan, Yuen T., Ngui, Siew Lin, Carne, Simon, Mbisa, Jean L.

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Very early lineage-specific chimerism after reduced intensity stem cell transplantation is highly predictive of clinical outcome for patients with myeloid disease von Kinsella, Francesca A.M., Inman, Charlotte F., Gudger, Amy, Chan, Yuen T., Murray, Duncan J., Zuo, Jianmin, McIlroy, Graham, Nagra, Sandeep, Nunnick, Jane, Holder, Kathy, Wall, Kerry, Griffiths, Mike, Craddock, Charles, Nikolousis, Emmanouil, Moss, Paul, Malladi, Ram

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Genomic autopsy to identify underlying causes of pregnancy loss and perinatal death von Byrne, Alicia B., Arts, Peer, Ha, Thuong T., Kassahn, Karin S., Pais, Lynn S., O’Donnell-Luria, Anne, Babic, Milena, Frank, Mahalia S. B., Feng, Jinghua, Wang, Paul, Lawrence, David M., Eshraghi, Leila, Arriola, Luis, Toubia, John, Nguyen, Hung, McGillivray, George, Pinner, Jason, McKenzie, Fiona, Morrow, Rebecca, Lipsett, Jill, Manton, Nick, Khong, T. Yee, Moore, Lynette, Liebelt, Jan E., Schreiber, Andreas W., King-Smith, Sarah L., Hardy, Tristan S. E., Jackson, Matilda R., Barnett, Christopher P., Scott, Hamish S.

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Author Correction: Genomic autopsy to identify underlying causes of pregnancy loss and perinatal death von Byrne, Alicia B., Arts, Peer, Ha, Thuong T., Kassahn, Karin S., Pais, Lynn S., O’Donnell-Luria, Anne, Babic, Milena, Frank, Mahalia S. B., Feng, Jinghua, Wang, Paul, Lawrence, David M., Eshraghi, Leila, Arriola, Luis, Toubia, John, Nguyen, Hung, McGillivray, George, Pinner, Jason, McKenzie, Fiona, Morrow, Rebecca, Lipsett, Jill, Manton, Nick, Khong, T. Yee, Moore, Lynette, Liebelt, Jan E., Schreiber, Andreas W., King-Smith, Sarah L., Hardy, Tristan S. E., Jackson, Matilda R., Barnett, Christopher P., Scott, Hamish S.

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Performance of Streck cfDNA Blood Collection Tubes for Liquid Biopsy Testing von Medina Diaz, Inga, Nocon, Annette, Mehnert, Daniel H, Fredebohm, Johannes, Diehl, Frank, Holtrup, Frank

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Measuring Digital PCR Quality: Performance Parameters and Their Optimization von Lievens, A, Jacchia, S, Kagkli, D, Savini, C, Querci, M

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The limits of personalization in precision medicine: Polygenic risk scores and racial categorization in a precision breast cancer screening trial von James, Jennifer Elyse, Riddle, Leslie, Koenig, Barbara Ann, Joseph, Galen

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Prognostic value of circulating tumor DNA in patients with colon cancer: Systematic review von Fan, Gaowei, Zhang, Kuo, Yang, Xin, Ding, Jiansheng, Wang, Zujian, Li, Jinming

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Non-invasive prenatal testing (NIPT) by low coverage genomic sequencing: Detection limits of screened chromosomal microdeletions von Kucharik, Marcel, Gnip, Andrej, Hyblova, Michaela, Budis, Jaroslav, Strieskova, Lucia, Harsanyova, Maria, Pös, Ondrej, Kubiritova, Zuzana, Radvanszky, Jan, Minarik, Gabriel, Szemes, Tomas

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Evaluation of molecular inversion probe versus TruSeq® custom methods for targeted next-generation sequencing von Almomani, Rowida, Marchi, Margherita, Sopacua, Maurice, Lindsey, Patrick, Salvi, Erika, Koning, Bart de, Santoro, Silvia, Magri, Stefania, Smeets, Hubert J M, Martinelli Boneschi, Filippo, Malik, Rayaz R, Ziegler, Dan, Hoeijmakers, Janneke G J, Bönhof, Gidon, Dib-Hajj, Sulayman, Waxman, Stephen G, Merkies, Ingemar S J, Lauria, Giuseppe, Faber, Catharina G, Gerrits, Monique M

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Evolution and taxonomic classification of human papillomavirus 16 (HPV16)-related variant genomes: HPV31, HPV33, HPV35, HPV52, HPV58 and HPV67 von Chen, Zigui, Schiffman, Mark, Herrero, Rolando, Desalle, Rob, Anastos, Kathryn, Segondy, Michel, Sahasrabuddhe, Vikrant V, Gravitt, Patti E, Hsing, Ann W, Burk, Robert D

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Echocardiographic findings in infants with presumed congenital Zika syndrome: Retrospective case series study von Cavalcanti, Danielle Di, Alves, Lucas V, Furtado, Geraldo J, Santos, Cleusa C, Feitosa, Fabiana G, Ribeiro, Maria C, Menge, Paulo, Lira, Izabelle M, Alves, Joao G

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Validation of a SNP-based non-invasive prenatal test to detect the fetal 22q11.2 deletion in maternal plasma samples von Ravi, Harini, McNeill, Gabriel, Goel, Shruti, Meltzer, Steven D, Hunkapiller, Nathan, Ryan, Allison, Levy, Brynn, Demko, Zachary P

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Non-invasive prenatal paternity testing by analysis of Y-chromosome mini-STR haplotype using next-generation sequencing von Song, Wenqian, Xiao, Nan, Zhou, Shihang, Yu, Weijian, Wang, Ni, Shao, Linnan, Duan, Ying, Chen, Mei, Pan, Lingzi, Xia, Yuexin, Zhang, Li, Liu, Ming

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Enrichment of circulating trophoblasts from maternal blood using filtration-based Metacell® technology von Weymaere, Jana, Vander Plaetsen, Ann-Sophie, Van Den Branden, Yasmine, Pospisilova, Eliska, Tytgat, Olivier, Deforce, Dieter, Van Nieuwerburgh, Filip

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Performance of Polymerase Chain Reaction Analysis of the Amniotic Fluid of Pregnant Women for Diagnosis of Congenital Toxoplasmosis: A Systematic Review and Meta-Analysis von de Oliveira Azevedo, Christianne Terra, do Brasil, Pedro Emmanuel A A, Guida, Letícia, Lopes Moreira, Maria Elizabeth

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Could Digital PCR Be an Alternative as a Non-Invasive Prenatal Test for Trisomy 21: A Proof of Concept Study von El Khattabi, Laïla Allach, Rouillac-Le Sciellour, Christelle, Le Tessier, Dominique, Luscan, Armelle, Coustier, Audrey, Porcher, Raphael, Bhouri, Rakia, Nectoux, Juliette, Sérazin, Valérie, Quibel, Thibaut, Mandelbrot, Laurent, Tsatsaris, Vassilis, Vialard, François, Dupont, Jean-Michel

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Modulation of cholesterol transport by maternal hypercholesterolemia in human full-term placenta von Zhang, Ran, Dong, Shan, Ma, Wei-Wei, Cai, Xue-Ping, Le, Zhi-Yin, Xiao, Rong, Zhou, Qi, Yu, Huan-Ling

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The contingent use of cell-free fetal DNA for prenatal screening of trisomies 21, 18, 13 in pregnant women within a national health service: A budget impact analysis von Prefumo, Federico, Paolini, Davide, Speranza, Giulia, Palmisano, Marilena, Dionisi, Matteo, Camurri, Lamberto

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