Lachlan James M. Coin

Orcid: 0000-0002-4300-455X

According to our database1, Lachlan James M. Coin authored at least 28 papers between 2004 and 2024.

Collaborative distances:
  • Dijkstra number2 of four.
  • Erdős number3 of four.

Timeline

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Bibliography

2024
PLANNER: A Multi-Scale Deep Language Model for the Origins of Replication Site Prediction.
IEEE J. Biomed. Health Informatics, April, 2024

2023
Digerati - A multipath parallel hybrid deep learning framework for the identification of mycobacterial PE/PPE proteins.
Comput. Biol. Medicine, September, 2023

TIMER is a Siamese neural network-based framework for identifying both general and species-specific bacterial promoters.
Briefings Bioinform., July, 2023

ATTIC is an integrated approach for predicting A-to-I RNA editing sites in three species.
Briefings Bioinform., May, 2023

2022
Nanoq: ultra-fast quality control for nanopore reads.
J. Open Source Softw., 2022

DeepGenGrep: a general deep learning-based predictor for multiple genomic signals and regions.
Bioinform., 2022

Critical assessment of computational tools for prokaryotic and eukaryotic promoter prediction.
Briefings Bioinform., 2022

Positive-unlabeled learning in bioinformatics and computational biology: a brief review.
Briefings Bioinform., 2022

2021
Real-time resolution of short-read assembly graph using ONT long reads.
PLoS Comput. Biol., 2021

Porpoise: a new approach for accurate prediction of RNA pseudouridine sites.
Briefings Bioinform., 2021

2018
npInv: accurate detection and genotyping of inversions using long read sub-alignment.
BMC Bioinform., 2018

GtTR: Bayesian estimation of absolute tandem repeat copy number using sequence capture and high throughput sequencing.
BMC Bioinform., 2018

Simulating the dynamics of targeted capture sequencing with CapSim.
Bioinform., 2018

2017
Real-time demultiplexing Nanopore barcoded sequencing data with npBarcode.
Bioinform., 2017

2016
Realtime analysis and visualization of MinION sequencing data with npReader.
Bioinform., 2016

2014
cnvOffSeq: detecting intergenic copy number variation using off-target exome sequencing data.
Bioinform., 2014

2013
YHap: a population model for probabilistic assignment of Y haplogroups from re-sequencing data.
BMC Bioinform., 2013

2012
An exome sequencing pipeline for identifying and genotyping common CNVs associated with disease with application to psoriasis.
Bioinform., 2012

2011
famCNV: copy number variant association for quantitative traits in families.
Bioinform., 2011

2010
Inferring combined CNV/SNP haplotypes from genotype data.
Bioinform., 2010

invertFREGENE: software for simulating inversions in population genetic data.
Bioinform., 2010

2008
TreeFam: 2008 Update.
Nucleic Acids Res., 2008

Inference of haplotypic phase and missing genotypes in polyploid organisms and variable copy number genomic regions.
BMC Bioinform., 2008

Disease association tests by inferring ancestral haplotypes using a hidden markov model.
Bioinform., 2008

2006
TreeFam: a curated database of phylogenetic trees of animal gene families.
Nucleic Acids Res., 2006

2004
The Pfam protein families database.
Nucleic Acids Res., 2004

Enhanced protein domain discovery using taxonomy.
BMC Bioinform., 2004

Improved techniques for the identification of pseudogenes.
Proceedings of the Proceedings Twelfth International Conference on Intelligent Systems for Molecular Biology/Third European Conference on Computational Biology 2004, 2004


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