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What is the expectation maximization algorithm?

Nature biotechnology, 2008-08, Vol.26 (8), p.897-899

2008

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Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease

PLoS genetics, 2011-06, Vol.7 (6), p.e1002141-e1002141

2011

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Genome-wide analysis points to roles for extracellular matrix remodeling, the visual cycle, and neuronal development in myopia

PLoS genetics, 2013-02, Vol.9 (2), p.e1003299-e1003299

2013

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Germ line variants predispose to both JAK2 V617F clonal hematopoiesis and myeloproliferative neoplasms

Blood, 2016-08, Vol.128 (8), p.1121-1128

2016

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Comparison of family history and SNPs for predicting risk of complex disease

PLoS genetics, 2012-10, Vol.8 (10), p.e1002973-e1002973

2012

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CONTRAfold: RNA secondary structure prediction without physics-based models

Bioinformatics, 2006-07, Vol.22 (14), p.e90-e98

2006

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Novel associations for hypothyroidism include known autoimmune risk loci

PloS one, 2012-04, Vol.7 (4), p.e34442-e34442

2012

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Serum iron levels and the risk of Parkinson disease: a Mendelian randomization study

PLoS medicine, 2013-06, Vol.10 (6), p.e1001462-e1001462

2013

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A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci

Nature genetics, 2013-08, Vol.45 (8), p.907-911

2013

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ProbCons: Probabilistic consistency-based multiple sequence alignment

Genome research, 2005-02, Vol.15 (2), p.330-340

2005

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Efficient replication of over 180 genetic associations with self-reported medical data

PloS one, 2011-08, Vol.6 (8), p.e23473-e23473

2011

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LAGAN and Multi-LAGAN: efficient tools for large-scale multiple alignment of genomic DNA

Genome research, 2003-04, Vol.13 (4), p.721-731

2003

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Glocal alignment: finding rearrangements during alignment

Bioinformatics, 2003-07, Vol.19 (suppl-1), p.i54-i62

2003

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A max-margin model for efficient simultaneous alignment and folding of RNA sequences

Bioinformatics, 2008-07, Vol.24 (13), p.i68-i76

2008

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CONTRAST: a discriminative, phylogeny-free approach to multiple informant de novo gene prediction

Genome biology, 2007-01, Vol.8 (12), p.R269-R269

2007

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Genetic variants associated with breast size also influence breast cancer risk

BMC medical genetics, 2012-06, Vol.13 (1), p.53-53, Article 53

2012

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Automated cellular annotation for high-resolution images of adult Caenorhabditis elegans

Bioinformatics, 2013-07, Vol.29 (13), p.i18-i26

2013

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Genetic variants associated with motion sickness point to roles for inner ear development, neurological processes and glucose homeostasis

Human molecular genetics, 2015-05, Vol.24 (9), p.2700-2708

2015

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Effect of genetic divergence in identifying ancestral origin using HAPAA

Genome Research, 2008-04, Vol.18 (4), p.676-682

2008

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CONTRAlign: Discriminative Training for Protein Sequence Alignment

Research in Computational Molecular Biology, p.160-174

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Automatic parameter learning for multiple local network alignment

Journal of computational biology, 2009-08, Vol.16 (8), p.1001-1022

2009

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Protein multiple sequence alignment

Methods in molecular biology (Clifton, N.J.), 2008, Vol.484, p.379

2008

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Multiple alignment of protein sequences with repeats and rearrangements

Nucleic acids research, 2006-11, Vol.34 (20), p.5932-5942

2006

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A Classifier-based approach to identify genetic similarities between diseases

Bioinformatics, 2009-06, Vol.25 (12), p.i21-i29

2009

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Correction: Serum Iron Levels and the Risk of Parkinson Disease: A Mendelian Randomization Study

PLoS medicine, 2013-06, Vol.10 (6)

2013

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What is the expectation maximization algorithm?

Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease

Genome-wide analysis points to roles for extracellular matrix remodeling, the visual cycle, and neuronal development in myopia

Germ line variants predispose to both JAK2 V617F clonal hematopoiesis and myeloproliferative neoplasms

Comparison of family history and SNPs for predicting risk of complex disease

CONTRAfold: RNA secondary structure prediction without physics-based models

Novel associations for hypothyroidism include known autoimmune risk loci

Serum iron levels and the risk of Parkinson disease: a Mendelian randomization study

A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci

ProbCons: Probabilistic consistency-based multiple sequence alignment

Efficient replication of over 180 genetic associations with self-reported medical data

LAGAN and Multi-LAGAN: efficient tools for large-scale multiple alignment of genomic DNA

Glocal alignment: finding rearrangements during alignment

A max-margin model for efficient simultaneous alignment and folding of RNA sequences

CONTRAST: a discriminative, phylogeny-free approach to multiple informant de novo gene prediction

Genetic variants associated with breast size also influence breast cancer risk

Automated cellular annotation for high-resolution images of adult Caenorhabditis elegans

Genetic variants associated with motion sickness point to roles for inner ear development, neurological processes and glucose homeostasis

Effect of genetic divergence in identifying ancestral origin using HAPAA

CONTRAlign: Discriminative Training for Protein Sequence Alignment

Automatic parameter learning for multiple local network alignment

Protein multiple sequence alignment

Multiple alignment of protein sequences with repeats and rearrangements

A Classifier-based approach to identify genetic similarities between diseases

Correction: Serum Iron Levels and the Risk of Parkinson Disease: A Mendelian Randomization Study

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