| 1263 | -- | 1268 | Roozbeh Dehghannasiri, Linda Szabo, Julia Salzman. Ambiguous splice sites distinguish circRNA and linear splicing in the human genome |
| 1269 | -- | 1277 | Yuchen Yang, Ruth Huh, Houston W. Culpepper, Yuan Lin, Michael I Love, Yun Li. SAFE-clustering: Single-cell Aggregated (from Ensemble) clustering for single-cell RNA-seq data |
| 1278 | -- | 1283 | Xuesi Dong, Lijuan Lin, Ruyang Zhang, Yang Zhao, David C. Christiani, Yongyue Wei, Feng Chen. TOBMI: trans-omics block missing data imputation using a k-nearest neighbor weighted approach |
| 1284 | -- | 1291 | Jaroslav Budis, Juraj Gazdarica, Jan Radvanszky, Gábor Szücs, Marcel Kucharík, Lucia Strieskova, Iveta Gazdaricova, Maria Harsanyova, Frantisek Duris, Gabriel Minarik, Martina Sekelska, Bálint Nagy, Jan Turna, Tomás Szemes. Combining count- and length-based z-scores leads to improved predictions in non-invasive prenatal testing |
| 1292 | -- | 1298 | Hussein Al-Asadi, Kushal K. Dey, John Novembre, Matthew Stephens. Inference and visualization of DNA damage patterns using a grade of membership model |
| 1299 | -- | 1309 | Chang Xu, Xiujing Gu, Raghavendra Padmanabhan, Zhong Wu, Quan Peng, John DiCarlo, Yexun Wang. smCounter2: an accurate low-frequency variant caller for targeted sequencing data with unique molecular identifiers |
| 1310 | -- | 1317 | Jaroslav Budis, Marcel Kucharík, Frantisek Duris, Juraj Gazdarica, Michaela Zrubcová, Andrej Ficek, Tomás Szemes, Brona Brejová, Jan Radvanszky. Dante: genotyping of known complex and expanded short tandem repeats |
| 1318 | -- | 1325 | Patrick V. Holec, Joseph Berleant, Mark Bathe, Michael E. Birnbaum. A Bayesian framework for high-throughput T cell receptor pairing |
| 1326 | -- | 1333 | Leyi Wei, Shasha Luan, Luis Augusto Eijy Nagai, Ran Su, Quan Zou. Exploring sequence-based features for the improved prediction of DNA N4-methylcytosine sites in multiple species |
| 1334 | -- | 1341 | Maciej Wójcikowski, Michal Kukielka, Marta M. Stepniewska-Dziubinska, Pawel Siedlecki. Development of a protein-ligand extended connectivity (PLEC) fingerprint and its application for binding affinity predictions |
| 1342 | -- | 1349 | Daniel Wiegreffe, Daniel Alexander, Peter F. Stadler, Dirk Zeckzer. RNApuzzler: efficient outerplanar drawing of RNA-secondary structures |
| 1350 | -- | 1357 | Kevin Y. X. Wang, Alexander M. Menzies, Ines P. Silva, James S. Wilmott, Yibing Yan, Matthew Wongchenko, Richard F. Kefford, Richard A. Scolyer, Georgina V. Long, Garth Tarr, Samuel Müller, Jean Y. H. Yang. bcGST - an interactive bias-correction method to identify over-represented gene-sets in boutique arrays |
| 1358 | -- | 1365 | Trang T. Le, Ryan J. Urbanowicz, Jason H. Moore, Brett A. McKinney. STatistical Inference Relief (STIR) feature selection |
| 1366 | -- | 1372 | Bin Guo, Baolin Wu. Powerful and efficient SNP-set association tests across multiple phenotypes using GWAS summary data |
| 1373 | -- | 1379 | Qiuying Sha, Zhenchuan Wang, Xiao Zhang, Shuanglin Zhang. A clustering linear combination approach to jointly analyze multiple phenotypes for GWAS |
| 1380 | -- | 1387 | Silvia Calderazzo, Marco Brancaccio, Bärbel Finkenstädt. Filtering and inference for stochastic oscillators with distributed delays |
| 1388 | -- | 1394 | Ishita K. Khan, Aashish Jain, Reda Rawi, Halima Bensmail, Daisuke Kihara. Prediction of protein group function by iterative classification on functional relevance network |
| 1395 | -- | 1403 | Yuan Luo, Chengsheng Mao, Yiben Yang, Fei Wang, Faraz S. Ahmad, Donna Arnett, Marguerite R. Irvin, Sanjiv J. Shah. Integrating hypertension phenotype and genotype with hybrid non-negative matrix factorization |
| 1404 | -- | 1413 | Albert Casanovas, Óscar Gallardo, Montserrat Carrascal, Joaquin Abian. TCellXTalk facilitates the detection of co-modified peptides for the study of protein post-translational modification cross-talk in T cells |
| 1414 | -- | 1415 | Cheng-Kai Shiau, Jia-Hsin Huang, Huai-Kuang Tsai. CATANA: a tool for generating comprehensive annotations of alternative transcript events |
| 1416 | -- | 1418 | Tuan Trieu, Oluwatosin Oluwadare, Julia Wopata, Jianlin Cheng. GenomeFlow: a comprehensive graphical tool for modeling and analyzing 3D genome structure |
| 1419 | -- | 1421 | Nengjun Yi, Zaixiang Tang, Xinyan Zhang, Boyi Guo. BhGLM: Bayesian hierarchical GLMs and survival models, with applications to genomics and epidemiology |
| 1422 | -- | 1424 | Evgeny Anatskiy, Devon Patrick Ryan, Björn A. Grüning, Laura Arrigoni, Thomas Manke, Ulrike Bönisch. Parkour LIMS: high-quality sample preparation in next generation sequencing |
| 1425 | -- | 1426 | Benjamin D. Lee. Squiggle: a user-friendly two-dimensional DNA sequence visualization tool |
| 1427 | -- | 1429 | Oana M. Enache, David L. Lahr, Ted E. Natoli, Lev Litichevskiy, David Wadden, Corey Flynn, Joshua Gould, Jacob K. Asiedu, Rajiv Narayan, Aravind Subramanian. The GCTx format and cmap{Py, R, M, J} packages: resources for optimized storage and integrated traversal of annotated dense matrices |
| 1430 | -- | 1432 | Xian Liu, Mingfei Han, Chen Zhao, Cheng Chang, Yunping Zhu, Changhui Ge, Ronghua Yin, Yiqun Zhan, Changyan Li, Miao Yu, Fuchu He, Xiaoming Yang. KeggExp: a web server for visual integration of KEGG pathways and expression profile data |
| 1433 | -- | 1435 | Junfang Chen, Dietmar Lippold, Josef Frank, William Rayner, Andreas Meyer-Lindenberg, Emanuel Schwarz. Gimpute: an efficient genetic data imputation pipeline |
| 1436 | -- | 1437 | Minoo Ashtiani, Mehdi Mirzaie, Mohieddin Jafari. CINNA: an R/CRAN package to decipher Central Informative Nodes in Network Analysis |
| 1438 | -- | 1440 | Yi Zhang, Mohith Manjunath, Yeonsung Kim, Joerg Heintz, Jun S. Song. SequencEnG: an interactive knowledge base of sequencing techniques |
| 1441 | -- | 1442 | Alejandro Brenes, Angus I. Lamond. The Encyclopedia of Proteome Dynamics: the KinoViewer |
| 1443 | -- | 0 | Bansho Masutani, Shinichi Morishita. A framework and an algorithm to detect low-abundance DNA by a handy sequencer and a palm-sized computer |