Martin Reese
Martin Reese
Fabric Genomics
Verified email at
Cited by
Cited by
The Genome Sequence of Drosophila melanogaster
MD Adams, SE Celniker, RA Holt, CA Evans, JD Gocayne, ...
Science 287 (5461), 2185-2195, 2000
Improved splice site detection in Genie
MG Reese, FH Eeckman, D Kulp, D Haussler
Journal of computational biology 4 (3), 311-323, 1997
Application of a time-delay neural network to promoter annotation in the Drosophila melanogaster genome
MG Reese
Computers & chemistry 26 (1), 51-56, 2001
Sequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encoding
KJ McKernan, HE Peckham, GL Costa, SF McLaughlin, Y Fu, EF Tsung, ...
Genome research 19 (9), 1527-1541, 2009
Assuring the quality of next-generation sequencing in clinical laboratory practice
AS Gargis, L Kalman, MW Berry, DP Bick, DP Dimmock, T Hambuch, F Lu, ...
Nature biotechnology 30 (11), 1033-1036, 2012
EGASP: the human ENCODE genome annotation assessment project
R Guigó, P Flicek, JF Abril, A Reymond, J Lagarde, F Denoeud, ...
Genome biology 7 (1), 1-31, 2006
An exploration of the sequence of a 2.9-Mb region of the genome of Drosophila melanogaster: the Adh region
M Ashburner, S Misra, J Roote, SE Lewis, R Blazej, T Davis, C Doyle, ...
Genetics 153 (1), 179-219, 1999
Genome annotation assessment in Drosophila melanogaster
MG Reese, G Hartzell, NL Harris, U Ohler, JF Abril, SE Lewis
Genome research 10 (4), 483-501, 2000
A probabilistic disease-gene finder for personal genomes
M Yandell, C Huff, H Hu, M Singleton, B Moore, J Xing, LB Jorde, ...
Genome research 21 (9), 1529-1542, 2011
Genie—gene finding in Drosophila melanogaster
MG Reese, D Kulp, H Tammana, D Haussler
Genome Research 10 (4), 529-538, 2000
Large scale sequencing specific neural networks for promoter and splice site recognition
MG Reese, NL Harris, FH Eeckman
Biocomputing: Proceedings of the 1996 pacific symposium, 737-738, 1996
Diagnosis of genetic diseases in seriously ill children by rapid whole-genome sequencing and automated phenotyping and interpretation
MM Clark, A Hildreth, S Batalov, Y Ding, S Chowdhury, K Watkins, ...
Science translational medicine 11 (489), eaat6177, 2019
Phevor combines multiple biomedical ontologies for accurate identification of disease-causing alleles in single individuals and small nuclear families
MV Singleton, SL Guthery, KV Voelkerding, K Chen, B Kennedy, ...
The American Journal of Human Genetics 94 (4), 599-610, 2014
VAAST 2.0: Improved variant classification and disease‐gene identification using a conservation‐controlled amino acid substitution matrix
H Hu, CD Huff, B Moore, S Flygare, MG Reese, M Yandell
Genetic epidemiology 37 (6), 622-634, 2013
Interpolated markov chains for eukaryotic promoter recognition.
U Ohler, S Harbeck, H Niemann, E Nö th, MG Reese
Bioinformatics (Oxford, England) 15 (5), 362-369, 1999
Annotating eukaryote genomes
S Lewis, M Ashburner, MG Reese
Current opinion in structural biology 10 (3), 349-354, 2000
Novel neural network algorithms for improved eukaryotic promoter site recognition
MG Reese, FH Eeckman
The Seventh International Genome Sequencing and Analysis Conference, Hilton …, 1995
100,000 genomes pilot on rare-disease diagnosis in health care—preliminary report
100,000 Genomes Project Pilot Investigators
New England Journal of Medicine 385 (20), 1868-1880, 2021
Population genetic inference from personal genome data: impact of ancestry and admixture on human genomic variation
JM Kidd, S Gravel, J Byrnes, A Moreno-Estrada, S Musharoff, K Bryc, ...
The American Journal of Human Genetics 91 (4), 660-671, 2012
An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge
CA Brownstein, AH Beggs, N Homer, B Merriman, TW Yu, KC Flannery, ...
Genome biology 15 (3), 1-18, 2014
The system can't perform the operation now. Try again later.
Articles 1–20