Search results for "NGS"

Hits ?▲	Authors	Title	Venue	Year	Link	Author keywords
107	Imen Grida Ben Yahia, Emmanuel Bertin, Noël Crespi	Towards autonomic management for Next Generation Services.	ICNS	2006	DBLP DOI BibTeX RDF	Next Generation Services (NGS), Autonomic computing, service management
79	Anita J. La Salle	Workshop 10 introduction: The Next Generation Software (NGS) workshop - NGS 2008.	IPDPS	2008	DBLP DOI BibTeX RDF
69	Imen Grida Ben Yahia, Emmanuel Bertin, Noël Crespi	Next/New Generation Networks Services and Management.	ICNS	2006	DBLP DOI BibTeX RDF	NGS, IMS, NGN, Service management
67	Vojtech Bystrý, Tomas Reigl, Adam Krejci, Martin Demko, Barbora Hanakova, Andrea Grioni, Henrik Knecht, Max Schlitt, Peter Dreger, Leopold Sellner, Dietrich Herrmann, Marine Pingeon, Myriam Boudjoghra, Jos Rijntjes, Christiane Pott, Anton W. Langerak, Patricia J. T. A. Groenen, Frederic Davi, Monika Brüggemann, Nikos Darzentas, EuroClonality-NGS	ARResT/Interrogate: an interactive immunoprofiler for IG/TR NGS data.	Bioinform.	2017	DBLP DOI BibTeX RDF
59	Daniele Braga, Diego Calvanese, Alessandro Campi, Stefano Ceri, Florian Daniel, Davide Martinenghi, Paolo Merialdo, Riccardo Torlone	NGS: a framework for multi-domain query answering.	ICDE Workshops	2008	DBLP DOI BibTeX RDF
58	Fereydoun Hormozdiari, Can Alkan, Evan E. Eichler, Süleyman Cenk Sahinalp	Combinatorial Algorithms for Structural Variation Detection in High Throughput Sequenced Genomes.	RECOMB	2009	DBLP DOI BibTeX RDF
58	David Spence, Neil Geddes, Jens Jensen, Andrew Richards, Matthew Viljoen, Andrew P. Martin, Matthew J. Dovey, Mark Norman, Kang Tang, Anne E. Trefethen, David Wallom, Rob Allan, David Meredith 0003	ShibGrid: Shibboleth Access for the UK National Grid Service.	e-Science	2006	DBLP DOI BibTeX RDF
58	Frederica Darema	The Next Generation Software Program.	Int. J. Parallel Program.	2005	DBLP DOI BibTeX RDF	Next Generation Software Program, TPES, CADSS
49	Imen Grida Ben Yahia, Emmanuel Bertin, Noël Crespi	Ontology-based Management Systems for the Next Generation Services: State-of-the-Art.	ICNS	2007	DBLP DOI BibTeX RDF	Next Generation Services (NGS), ontology, Next Generation Networks, Enterprise Information System, service delivery
47	Bastian Schiffthaler, Myrto Kostadima, NGS Trainer Consortium, Nicolas Delhomme, Gabriella Rustici	Training in High-Throughput Sequencing: Common Guidelines to Enable Material Sharing, Dissemination, and Reusability.	PLoS Comput. Biol.	2016	DBLP DOI BibTeX RDF
40	Tiffany Delhomme	Using the systematic nature of errors in NGS data to efficiently detect mutations : computational methods and application to early cancer detection. (Utiliser la nature systématique des erreurs dans les données NGS pour détecter efficacement les mutations : méthodes de calcul et application à la détection précoce du cancer).		2019	RDF
40	Leandro Ishi Soares de Lima	De novo algorithms to identify patterns associated with biological events in de Bruijn graphs built from NGS data. (Algorithmes de novo pour l'identification de motifs associés à des événements biologiques dans les graphes de De Bruijn construits à partir de données NGS).		2019	RDF
40	Jochen Singer, Hans-Joachim Ruscheweyh, Ariane L. Hofmann, Thomas Thurnherr, Franziska Singer, Nora C. Toussaint, Charlotte K. Y. Ng, Salvatore Piscuoglio, Christian Beisel, Gerhard Christofori, Reinhard Dummer, Michael N. Hall, Wilhelm Krek, Mitchell P. Levesque, Markus G. Manz, Holger Moch, Andreas Papassotiropoulos, Daniel J. Stekhoven, Peter Wild, Thomas Wüst, Bernd Rinn, Niko Beerenwinkel	NGS-pipe: a flexible, easily extendable and highly configurable framework for NGS analysis.	Bioinform.	2018	DBLP DOI BibTeX RDF
40	Viola Ravasio, Marco Ritelli, Andrea Legati, Edoardo Giacopuzzi	GARFIELD-NGS: Genomic vARiants FIltering by dEep Learning moDels in NGS.	Bioinform.	2018	DBLP DOI BibTeX RDF
40	Ruoyan Chen	A new tool for detecting short inversions using next generation sequencing (NGS) data and a systematic comparison of different NGS platforms on detection sensitivities.		2017	RDF
40	Elise Ruark, Anthony Renwick, Matthew Clarke, Katie Snape, Emma Ramsay, Anna Elliott, Sandra Hanks, Ann Strydom, Sheila Seal, Nazneen Rahman	The ICR142 NGS validation series: a resource for orthogonal assessment of NGS analysis.	F1000Research	2016	DBLP DOI BibTeX RDF
40	Amin Ardeshirdavani, Erika L. Souche, Luc Dehaspe, Jeroen K. J. Van Houdt, Joris Robert Vermeesch, Yves Moreau	NGS-Logistics: data infrastructure for efficient analysis of NGS sequence variants across multiple centers.	BMC Bioinform.	2015	DBLP DOI BibTeX RDF
40	Ali May, Sanne Abeln, Mark J. Buijs, Jaap Heringa, Wim Crielaard, Bernd W. Brandt	NGS-eval: NGS Error analysis and novel sequence VAriant detection tooL.	Nucleic Acids Res.	2015	DBLP DOI BibTeX RDF
40	Andreea Radulescu	Assemblage de novo de répétitions à partir de données NGS. (De novo repeat assembly from NGS data).		2015	RDF
39	Paul Medvedev, Michael Brudno	Ab Initio Whole Genome Shotgun Assembly with Mated Short Reads.	RECOMB	2008	DBLP DOI BibTeX RDF
39	Frederica Darema	The Next Generation Software Workshop - IPDPS'07.	IPDPS	2007	DBLP DOI BibTeX RDF
39	Neil Geddes	The National Grid Service of the UK.	e-Science	2006	DBLP DOI BibTeX RDF
30	Emmanuel Bertin, Noël Crespi	Service business processes for the next generation of services: a required step to achieve service convergence.	Ann. des Télécommunications	2009	DBLP DOI BibTeX RDF	NGS, Service enabler, Business process, Service modeling
20	Rituparna Sinha, Rajat Kumar Pal, Rajat K. De	ENLIGHTENMENT: A Scalable Annotated Database of Genomics and NGS-Based Nucleotide Level Profiles.	IEEE ACM Trans. Comput. Biol. Bioinform.	2024	DBLP DOI BibTeX RDF
20	Amira Sami, Sara El-Metwally, M. Z. Rashad	MAC-ErrorReads: machine learning-assisted classifier for filtering erroneous NGS reads.	BMC Bioinform.	2024	DBLP DOI BibTeX RDF
20	A. K. M. Tauhidul Islam, Sakti Pramanik	Fast Edit Distance Prediction for All Pairs of Sequences in Very Large NGS Datasets.	PKDD (4)	2024	DBLP DOI BibTeX RDF
20	Ye Chen, Yuyan Wang, Ping Zhou, Hao Huang, Rui Li, Zhen Zeng, Zifeng Cui, Rui Tian, Zhuang Jin, Jiashuo Liu, Zhaoyue Huang, Lifang Li, Zheying Huang, Xun Tian, Meiying Yu, Zheng Hu	VIS Atlas: A Database of Virus Integration Sites in Human Genome from NGS Data to Explore Integration Patterns.	Genom. Proteom. Bioinform.	2023	DBLP DOI BibTeX RDF
20	Chunjiang Yu, Xin Qi, Wenying Yan, Wentao Wu 0004, Bairong Shen	Next-Generation Sequencing Markup Language (NGSML): A Medium for the Representation and Exchange of NGS Data.	IEEE ACM Trans. Comput. Biol. Bioinform.	2023	DBLP DOI BibTeX RDF
20	Qun-ting Lin, Wei Yang, Xin Zhang, Qi-gang Li, Yong-feng Liu, Qin Yan, Lei Sun	Systematic and benchmarking studies of pipelines for mammal WGBS data in the novel NGS platform.	BMC Bioinform.	2023	DBLP DOI BibTeX RDF
20	Óscar Castellanos-Rodríguez, Roberto R. Expósito, Juan Touriño	SeQual-Stream: approaching stream processing to quality control of NGS datasets.	BMC Bioinform.	2023	DBLP DOI BibTeX RDF
20	Marc Vaisband, Maria Schubert, Franz Josef Gassner, Roland Geisberger, Richard Greil, Nadja Zaborsky, Jan Hasenauer	Validation of genetic variants from NGS data using deep convolutional neural networks.	BMC Bioinform.	2023	DBLP DOI BibTeX RDF
20	Yabing Song, Jianbin Wang	ggcoverage: an R package to visualize and annotate genome coverage for various NGS data.	BMC Bioinform.	2023	DBLP DOI BibTeX RDF
20	Maksim S. Makarenko, Vera A. Gavrilova	NGS Reads Dataset of Sunflower Interspecific Hybrids.	Data	2023	DBLP DOI BibTeX RDF
20	Ajay Anand Kumar, Bart Loeys, Gerarda Van De Beek, Nils Peeters, Wim Wuyts, Lut Van Laer, Geert Vandeweyer, Maaike Alaerts	varAmpliCNV: analyzing variance of amplicons to detect CNVs in targeted NGS data.	Bioinform.	2023	DBLP DOI BibTeX RDF
20	Martin Wegner, Manuel Kaulich	ReCo: automated NGS re ad- co unting of single and combinatorial CRISPR gRNAs.	Bioinform.	2023	DBLP DOI BibTeX RDF
20	Riccardo Scandino, Federico Calabrese, Alessandro Romanel	Synggen: fast and data-driven generation of synthetic heterogeneous NGS cancer data.	Bioinform.	2023	DBLP DOI BibTeX RDF
20	Alberto Mulone, Sherine Awad, Davide Chiarugi, Marco Aldinucci	Porting the Variant Calling Pipeline for NGS data in cloud-HPC environment.	COMPSAC	2023	DBLP DOI BibTeX RDF
20	Emanuele Marchi, Mathew Jones, Paul Klenerman, John Frater, Gkikas Magiorkinis, Robert Belshaw	BreakAlign: a Perl program to align chimaeric (split) genomic NGS reads and allow visual confirmation of novel retroviral integrations.	BMC Bioinform.	2022	DBLP DOI BibTeX RDF
20	Juhyeon Kim, Saeyeon Cheon, Insung Ahn	NGS data vectorization, clustering, and finding key codons in SARS-CoV-2 variations.	BMC Bioinform.	2022	DBLP DOI BibTeX RDF
20	Julia Vetter, Susanne Schaller, Andreas Heinzel, Constantin Aschauer, Roman Reindl-Schwaighofer, Kira Jelencsics, Karin Hu, Rainer Oberbauer, Stephan M. Winkler	ImmunoDataAnalyzer: a bioinformatics pipeline for processing barcoded and UMI tagged immunological NGS data.	BMC Bioinform.	2022	DBLP DOI BibTeX RDF
20	Konstantina Koliogeorgi, Sotirios Xydis, Georgi Gaydadjiev, Dimitrios Soudris	GANDAFL: Dataflow Acceleration for Short Read Alignment on NGS Data.	IEEE Trans. Computers	2022	DBLP DOI BibTeX RDF
20	Meng-Huan Song, Chaochao Yan, Jiatang Li	MEANGS: an efficient seed-free tool for de novo assembling animal mitochondrial genome using whole genome NGS data.	Briefings Bioinform.	2022	DBLP DOI BibTeX RDF
20	Melivoia Rapti, Yassine Zouaghi, Jenny Meylan, Emmanuelle Ranza, Stylianos E. Antonarakis, Federico Andrea Santoni	CoverageMaster: comprehensive CNV detection and visualization from NGS short reads for genetic medicine applications.	Briefings Bioinform.	2022	DBLP DOI BibTeX RDF
20	Haque A. K. Alvi, Kun Xie, Kang Liu, Haiyong Zhao, Xiaohui Yang, Xiguo Yuan	Detection of copy number variations from NGS data by using an adaptive kernel density estimation-based outlier factor.	Digit. Signal Process.	2022	DBLP DOI BibTeX RDF
20	Vinzenz May, Leonard Koch, Björn Fischer-Zirnsak, Denise Horn, Petra Gehle, Uwe Kornak, Dieter Beule, Manuel Holtgrewe	ClearCNV: CNV calling from NGS panel data in the presence of ambiguity and noise.	Bioinform.	2022	DBLP DOI BibTeX RDF
20	Alissa L. Severson, Thorfinn Sand Korneliussen, Ida Moltke	LocalNgsRelate: a software tool for inferring IBD sharing along the genome between pairs of individuals from low-depth NGS data.	Bioinform.	2022	DBLP DOI BibTeX RDF
20	Xuan Wang, Junqing Li, Tihao Huang	CNVABNN: An AdaBoost algorithm and neural networks-based detection of copy number variations from NGS data.	Comput. Biol. Chem.	2022	DBLP DOI BibTeX RDF
20	Emilia Ståhlbom, Jesper Molin, Claes Lundström, Anders Ynnerman	Visualization Challenges of Variant Interpretation in Multiscale NGS Data.	EuroVis (Posters)	2022	DBLP DOI BibTeX RDF
20	Ram Nageena Singh, Etienne Z. Gnimpieba, Rajesh Kumar Sani	Title: Challenges in single cells sequencing Microbial community and biofilm: A case of Oleidesulfovibrio alaskensis G20 NGS protocol.	BIBM	2022	DBLP DOI BibTeX RDF
20	Thomas Krannich	Contributions to the detection of non-reference sequences in population-scale NGS data		2022	RDF
20	Luigi Donato, Concetta Scimone, Carmela Rinaldi, Rosalia D'Angelo, Antonina Sidoti	New evaluation methods of read mapping by 17 aligners on simulated and empirical NGS data: an updated comparison of DNA- and RNA-Seq data from Illumina and Ion Torrent technologies.	Neural Comput. Appl.	2021	DBLP DOI BibTeX RDF
20	Xiguo Yuan, Junping Li, Jun Bai, Jianing Xi	A Local Outlier Factor-Based Detection of Copy Number Variations From NGS Data.	IEEE ACM Trans. Comput. Biol. Bioinform.	2021	DBLP DOI BibTeX RDF
20	Maria Zanti, Kyriaki Michailidou, Maria Loizidou, Christina Machattou, Panagiota Pirpa, Kyproula Christodoulou, George M. Spyrou, Kyriacos Kyriacou, Andreas Hadjisavvas	Performance evaluation of pipelines for mapping, variant calling and interval padding, for the analysis of NGS germline panels.	BMC Bioinform.	2021	DBLP DOI BibTeX RDF
20	Ryan D. Kuster, G. Craig Yencho, Bode A. Olukolu	ngsComposer: an automated pipeline for empirically based NGS data quality filtering.	Briefings Bioinform.	2021	DBLP DOI BibTeX RDF
20	E. Sacristán-Horcajada, S. González-de la Fuente, R. Peiró-Pastor, Fernando Carrasco-Ramiro, R. Amils, J. M. Requena, J. Berenguer, B. Aguado	ARAMIS: From systematic errors of NGS long reads to accurate assemblies.	Briefings Bioinform.	2021	DBLP DOI BibTeX RDF
20	José Marcos Moreno-Cabrera, Jesús del Valle, Elisabeth Castellanos, Lidia Feliubadaló, Marta Pineda, Eduard Serra, Gabriel Capellá, Conxi Lázaro, Bernat Gel	CNVfilteR: an R/Bioconductor package to identify false positives produced by germline NGS CNV detection tools.	Bioinform.	2021	DBLP DOI BibTeX RDF
20	Filippo Geraci, Giovanni Manzini	EZcount: An all-in-one software for microRNA expression quantification from NGS sequencing data.	Comput. Biol. Medicine	2021	DBLP DOI BibTeX RDF
20	Giannis Mouchakis, Babis Kostopoulos, Stasinos Konstantopoulos, Ilias Kanellos, Anargiros Tzerefos, Thanasis Vergoulis, Thodoris Dalamagas 0001	A Cloud-Native NGS Data Processing and Annotation Platform.	Poly/DMAH@VLDB	2021	DBLP DOI BibTeX RDF
20	Mohamad Suhel Dalati, Weizhi Meng 0001, Wei-Yang Chiu	NGS: Mitigating DDoS Attacks using SDN-based Network Gate Shield.	GLOBECOM	2021	DBLP DOI BibTeX RDF
20	Christos V. Bellos, Alexandros Fyraridis, Georgios Stergios, Konstantinos Stefanou	An intelligent genetic platform diagnosing DNA sequencing pathogens by using NGS.	SEEDA-CECNSM	2021	DBLP DOI BibTeX RDF
20	Felipe Vaz Peres, Diego Mauricio Riaño-Pachón	ContFree-NGS: Removing Reads from Contaminating Organisms in Next Generation Sequencing Data.	BSB	2021	DBLP DOI BibTeX RDF
20	Roberto R. Expósito, Roi Galego-Torreiro, Jorge González-Domínguez	SeQual: Big Data Tool to Perform Quality Control and Data Preprocessing of Large NGS Datasets.	IEEE Access	2020	DBLP DOI BibTeX RDF
20	Madhumitha Ramamurthy, Ilango Krishnamurthi, S. Vimal 0001, Yesudhas Harold Robinson	Deep learning based genome analysis and NGS-RNA LL identification with a novel hybrid model.	Biosyst.	2020	DBLP DOI BibTeX RDF
20	Xingyu Liao, Min Li 0007, You Zou, Fang-Xiang Wu, Yi Pan 0001, Jianxin Wang 0001	An Efficient Trimming Algorithm based on Multi-Feature Fusion Scoring Model for NGS Data.	IEEE ACM Trans. Comput. Biol. Bioinform.	2020	DBLP DOI BibTeX RDF
20	Dan Wang, Hai Xiang, Chao Ning, Hao Liu, Jian-Feng Liu, Xingbo Zhao	Mitochondrial DNA enrichment reduced NUMT contamination in porcine NGS analyses.	Briefings Bioinform.	2020	DBLP DOI BibTeX RDF
20	Frédéric Escudié, Charles Van Goethem, David Grand, Julie Vendrell, Anna Vigier, Pierre Brousset, Solène M. Evrard, Jérôme Solassol, Janick Selves	MIAmS: microsatellite instability detection on NGS amplicons data.	Bioinform.	2020	DBLP DOI BibTeX RDF
20	Vincent Sater, Pierre-Julien Viailly, Thierry Lecroq, Élise Prieur-Gaston, Élodie Bohers, Mathieu Viennot, Philippe Ruminy, Hélène Dauchel, Pierre Vera, Fabrice Jardin	UMI-VarCal: a new UMI-based variant caller that efficiently improves low-frequency variant detection in paired-end sequencing NGS libraries.	Bioinform.	2020	DBLP DOI BibTeX RDF
20	Gianvito Urgese, Emanuele Parisi, Orazio M. Scicolone, Santa Di Cataldo, Elisa Ficarra	BioSeqZip: a collapser of NGS redundant reads for the optimization of sequence analysis.	Bioinform.	2020	DBLP DOI BibTeX RDF
20	Christopher M. Ward, Thu-Hien To, Stephen M. Pederson	ngsReports: a Bioconductor package for managing FastQC reports and other NGS related log files.	Bioinform.	2020	DBLP DOI BibTeX RDF
20	Weibo Zheng, Jing Chen, Thomas G. Doak, Weibo Song, Ying Yan	ADFinder: accurate detection of programmed DNA elimination using NGS high-throughput sequencing data.	Bioinform.	2020	DBLP DOI BibTeX RDF
20	Rongshan Yu, Wenxian Yang	ScaleQC: a scalable lossy to lossless solution for NGS data compression.	Bioinform.	2020	DBLP DOI BibTeX RDF
20	Nils Koelling, Marie Bernkopf, Eduardo Calpena, Geoffrey J. Maher, Kerry A. Miller, Hannah K. Ralph, Anne Goriely, Andrew O. M. Wilkie	amplimap: a versatile tool to process and analyze targeted NGS data.	Bioinform.	2020	DBLP DOI BibTeX RDF
20	Christopher Schiefer, Marc Bux, Jörgen Brandt, Clemens Messerschmidt, Knut Reinert, Dieter Beule, Ulf Leser	Portability of Scientific Workflows in NGS Data Analysis: A Case Study.	CoRR	2020	DBLP BibTeX RDF
20	Andrey Kechin, Viktoria Borobova, Ulyana Boyarskikh, Evgeniy Khrapov, Sergey Subbotin 0003, Maxim Filipenko	NGS-PrimerPlex: High-throughput primer design for multiplex polymerase chain reactions.	PLoS Comput. Biol.	2020	DBLP DOI BibTeX RDF
20	Tomasz Ploszaj, Karolina Antosik, Paulina Mludzik, Magdalena Traczyk-Borszynska, Maciej Borowiec	Clinical use of NGS data from the targeted gene panel for mitochondrial diseases screening.	Comput. Methods Programs Biomed.	2020	DBLP DOI BibTeX RDF
20	Marcus Braga, Kenny Pinheiro, Fabrício Almeida Araújo, Fábio Miranda 0002, Artur Silva, Rommel Ramos	Redundancy Treatment of NGS Contigs in Microbial Genome Finishing with Hashing-Based Approach.	BSB	2020	DBLP DOI BibTeX RDF
20	Fengfeng Luo, Yue Fu, Yongrong Qin	Diversity Analysis Based on BP Neural Network and NGS Algorithm.	ATCI	2020	DBLP DOI BibTeX RDF
20	Phanucheep Chotnithi	Efficient Similarity Measures in NGS Genome Data Comparison for Phylogeny Reconstruction.		2020	RDF
20	Christian Wünsch	AMLVaran: a software approach to implement variant analysis of targeted NGS sequencing data in an oncological care setting.		2020	RDF
20	Ahmed Ibrahim Samir Khalil	Digital karyotyping of cancer cell lines from NGS data		2020	DOI RDF
20	Phanucheep Chotnithi, Hong Van Le, Atsuhiro Takasu	An Effective Parameter-free Comparison of NGS Short Reads for Phylogeny Reconstruction.	J. Inf. Process.	2019	DBLP DOI BibTeX RDF
20	Sandip Samaddar, Rituparna Sinha, Rajat K. De	A Model for Distributed Processing and Analyses of NGS Data under Map-Reduce Paradigm.	IEEE ACM Trans. Comput. Biol. Bioinform.	2019	DBLP DOI BibTeX RDF
20	Alfredo Iacoangeli, Ahmad Al Khleifat, William Sproviero, Aleksey Shatunov, A. R. Jones, S. L. Morgan, Alan Pittman, Richard J. B. Dobson, S. J. Newhouse, Ammar Al-Chalabi	DNAscan: personal computer compatible NGS analysis, annotation and visualisation.	BMC Bioinform.	2019	DBLP DOI BibTeX RDF
20	Shifu Chen, Yanqing Zhou, Yaru Chen, Tanxiao Huang, Wenting Liao, Yun Xu, Zhicheng Li 0001, Jia Gu	Gencore: an efficient tool to generate consensus reads for error suppressing and duplicate removing of NGS data.	BMC Bioinform.	2019	DBLP DOI BibTeX RDF
20	Mara Sangiovanni, Ilaria Granata, Amarinder Singh Thind, Mario Rosario Guarracino	From trash to treasure: detecting unexpected contamination in unmapped NGS data.	BMC Bioinform.	2019	DBLP DOI BibTeX RDF
20	Nauman Ahmed, Jonathan Levy, Shanshan Ren, Hamid Mushtaq, Koen Bertels, Zaid Al-Ars	Correction to: GASAL2: a GPU accelerated sequence alignment library for high-throughput NGS data.	BMC Bioinform.	2019	DBLP DOI BibTeX RDF
20	Taewoon Joo, Ji-Hye Choi, Ji-Hye Lee, So Eun Park, Youngsic Jeon, Sae Hoon Jung, Hyun Goo Woo	SEQprocess: a modularized and customizable pipeline framework for NGS processing in R package.	BMC Bioinform.	2019	DBLP DOI BibTeX RDF
20	Nauman Ahmed, Jonathan Levy, Shanshan Ren, Hamid Mushtaq, Koen Bertels, Zaid Al-Ars	GASAL2: a GPU accelerated sequence alignment library for high-throughput NGS data.	BMC Bioinform.	2019	DBLP DOI BibTeX RDF
20	Hein Chun, Sangwoo Kim	BAMixChecker: an automated checkup tool for matched sample pairs in NGS cohort.	Bioinform.	2019	DBLP DOI BibTeX RDF
20	Nils Koelling, Marie Bernkopf, Eduardo Calpena, Geoffrey J. Maher, Kerry A. Miller, Hannah K. Ralph, Anne Goriely, Andrew O. M. Wilkie	amplimap: a versatile tool to process and analyze targeted NGS data.	Bioinform.	2019	DBLP DOI BibTeX RDF
20	Romain Groux, Philipp Bucher	SPar-K: a method to partition NGS signal data.	Bioinform.	2019	DBLP DOI BibTeX RDF
20	Yuan Liu, Yongchao Ma, Evan Salsman, Frank A. Manthey, Elias M. Elias, Xuehui Li, Changhui Yan	An enrichment method for mapping ambiguous reads to the reference genome for NGS analysis.	J. Bioinform. Comput. Biol.	2019	DBLP DOI BibTeX RDF
20	Sanjeev Kumar, Suneeta Agarwal, Ranvijay	Fast and memory efficient approach for mapping NGS reads to a reference genome.	J. Bioinform. Comput. Biol.	2019	DBLP DOI BibTeX RDF
20	Shenjie Wang, Jiayin Wang, Xiao Xiao, Xuanping Zhang, Xuwen Wang, Xiaoyan Zhu 0003, Xin Lai 0003	GSDcreator: An Efficient and Comprehensive Simulator for Genarating NGS Data with Population Genetic Information.	BIBM	2019	DBLP DOI BibTeX RDF
20	Michael G. Sadovsky, Victory Kobets, Georgy Khodos, Dmitry A. Kuzmin, Vadim V. Sharov	Reads in NGS Are Distributed over a Sequence Very Inhomogeneously.	IWBBIO (1)	2019	DBLP DOI BibTeX RDF
20	Feng Gao, Liwei Gao, Jing-Yang Gao	Integrated Detection of Copy Number Variation Based on the Assembly of NGS and 3GS Data.	IWBBIO (1)	2019	DBLP DOI BibTeX RDF
20	Sean K. Lachhander, John Ziegler, Shoham Das, Paulo Salazar, Nana Mensah, Ivelise Rijo, Lissette Fernandez, Lin Dong, Daniela Elezovic, Ahmet Zehir, Maria Arcila	MPath Non-NGS: Software for Analysis of Clinical Fragment and Qualitative Polymerase Chain Reaction (PCR) Assays.	AMIA	2019	DBLP BibTeX RDF
20	Chao-Jung Wu, Amine M. Remita, Abdoulaye Baniré Diallo	MirLibSpark: A Scalable NGS Plant MicroRNA Prediction Pipeline for Multi-Library Functional Annotation.	BCB	2019	DBLP DOI BibTeX RDF
20	Alexis Robitaille	Detection and identification of papillomavirus sequences in NGS data of human DNA samples : a bioinformatic approach. (Détection et identification de séquences de papillomavirus dans des données de séquençage de nouvelle génération d'échantillons humain d'ADN : une approche bioinformatique).		2019	RDF
20	Alexander Seitz	Methods to improve short fragment NGS analysis - with a focus on ancient DNA		2019	RDF