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BMC Genomics, Volume 14 - Supplements
Volume 14, Number S-1, January 2013
Proceedings
- Quan Chen, Fengzhu Sun:
A unified approach for allele frequency estimation, SNP detection and association studies based on pooled sequencing data using EM algorithms. S1 - Chih-Hung Chou, Feng-Mao Lin, Min-Te Chou, Sheng-Da Hsu, Tzu-Hao Chang, Shun-Long Weng, Sirjana Shrestha, Chiung-Chih Hsiao, Jui-Hung Hung, Hsien-Da Huang:
A computational approach for identifying microRNA-target interactions using high-throughput CLIP and PAR-CLIP sequencing. S2 - W. Evan Durno, Niels W. Hanson, Kishori M. Konwar, Steven J. Hallam:
Expanding the boundaries of local similarity analysis. S3 - Zhen Gao, Ruizhe Zhao, Jianhua Ruan:
A genome-wide cis-regulatory element discovery method based on promoter sequences and gene co-expression networks. S4 - Trupti Joshi, Babu Valliyodan, Jeng-Hung Wu, Suk-Ha Lee, Dong Xu, Henry T. Nguyen:
Genomic differences between cultivated soybean, G. max and its wild relative G. soja. S5 - Minho Lee, Sangjo Han, Hyeshik Chang, Youn-Sig Kwak, David M. Weller, Dongsup Kim:
FitSearch: a robust way to interpret a yeast fitness profile in terms of drug's mode-of-action. S6 - Sergey I. Nikolenko, Anton I. Korobeynikov, Max A. Alekseyev:
BayesHammer: Bayesian clustering for error correction in single-cell sequencing. S7 - Nathaniel Parrish, Benjamin Sudakov, Eleazar Eskin:
Genome reassembly with high-throughput sequencing data. S8 - Ellis Patrick, Michael J. Buckley, David M. Lin, Yee Hwa Yang:
Improved moderation for gene-wise variance estimation in RNA-Seq via the exploitation of external information. S9 - Filippo Utro, Marc Pybus, Laxmi Parida:
Sum of parts is greater than the whole: inference of common genetic history of populations. S10 - Jiayin Wang, Zhongmeng Zhao, Zhi Cao, Aiyuan Yang, Jin Zhang:
A probabilistic method for identifying rare variants underlying complex traits. S11 - Roland Wittler:
Unraveling overlapping deletions by agglomerative clustering. S12 - Hongyi Xin, Donghyuk Lee, Farhad Hormozdiari, Samihan Yedkar, Onur Mutlu, Can Alkan:
Accelerating read mapping with FastHASH. S13 - Habil Zare, Gholamreza Haffari, Arvind Gupta, Ryan Remy Brinkman:
Scoring relevancy of features based on combinatorial analysis of Lasso with application to lymphoma diagnosis. S14 - Jia Zeng, Sridhar Hannenhalli:
Inferring evolution of gene duplicates using probabilistic models and nonparametric belief propagation. S15
- Roland Wittler:
Correction: Unraveling overlapping deletions by agglomerative clustering. S16
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