Larry Croft

Prof. Larry Croft

Genomics & Manager, Deakin Genomics Research and Discovery Facility, Deakin University, Geelong, Australia
orcid

Research Focus & Metrics

Academic Career Length

14Years (2013-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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12 January 2018 in GigaScience
Verified
Journal Article
Open access
PDF file
MTMun Hua Tan
Mun Hua Tan
CAChristopher M Austin
Christopher M Austin
MHMichael P Hammer
Michael P Hammer
YLYin Peng Lee
Yin Peng Lee
LCLarry Croft
Larry Croft
HGHan Ming Gan
Han Ming Gan
Some of the most widely recognized coral reef fishes are clownfish or anemonefish, members of the family Pomacentridae (subfamily: Amphiprioninae). They are popular aquarium species due to their bright colours, adaptability to captivity, and fascinating behavior. Their breeding biology (sequential hermaphrodites) and symbiotic mutualism with sea anemones have attracted much scientific interest. Moreover, there are some curious geographic-based phenotypes that warrant investigation. Leveraging on the advancement in Nanopore long read technology, we report the first hybrid assembly of the clown anemonefish (Amphiprion ocellaris) genome utilizing Illumina and Nanopore reads, further demonstrating the substantial impact of modest long read sequencing data sets on improving genome assembly statistics. We generated 43 Gb of short Illumina reads and 9 Gb of long Nanopore reads, representing approximate genome coverage of 54× and 11×, respectively, based on the range of estimated k-mer-predicted genome sizes of between 791 and 967 Mbp. The final assembled genome is contained in 6404 scaffolds with an accumulated length of 880 Mb (96.3% BUSCO-calculated genome completeness). Compared with the Illumina-only assembly, the hybrid approach generated 94% fewer scaffolds with an 18-fold increase in N50 length (401 kb) and increased the genome completeness by an additional 16%. A total of 27 240 high-quality protein-coding genes were predicted from the clown anemonefish, 26 211 (96%) of which were annotated functionally with information from either sequence homology or protein signature searches. We present the first genome of any anemonefish and demonstrate the value of low coverage (∼11×) long Nanopore read sequencing in improving both genome assembly contiguity and completeness. The near-complete assembly of the A. ocellaris genome will be an invaluable molecular resource for supporting a range of genetic, genomic, and phylogenetic studies specifically for clownfish and more generally for other related fish species of the family Pomacentridae.

19 July 2017 in GigaScience
Verified
Journal Article
Open access
PDF file
CAChristopher M. Austin
Christopher M. Austin
MTMun Hua Tan
Mun Hua Tan
KHKatherine A. Harrisson
Katherine A. Harrisson
YLYin Peng Lee
Yin Peng Lee
LCLarry Croft
Larry Croft
HGHan Ming Gan
Han Ming Gan
One of the most iconic Australian fish is the Murray cod, Maccullochella peelii (Mitchell 1838), a freshwater species that can grow to ∼1.8 metres in length and live to age ≥48 years. The Murray cod is of a conservation concern as a result of strong population contractions, but it is also popular for recreational fishing and is of growing aquaculture interest. In this study, we report the whole genome sequence of the Murray cod to support ongoing population genetics, conservation, and management research, as well as to better understand the evolutionary ecology and history of the species. A draft Murray cod genome of 633 Mbp (N50 = 109 974bp; BUSCO and CEGMA completeness of 94.2% and 91.9%, respectively) with an estimated 148 Mbp of putative repetitive sequences was assembled from the combined sequencing data of 2 fish individuals with an identical maternal lineage; 47.2 Gb of Illumina HiSeq data and 804 Mb of Nanopore data were generated from the first individual while 23.2 Gb of Illumina MiSeq data were generated from the second individual. The inclusion of Nanopore reads for scaffolding followed by subsequent gap-closing using Illumina data led to a 29% reduction in the number of scaffolds and a 55% and 54% increase in the scaffold and contig N50, respectively. We also report the first transcriptome of Murray cod that was subsequently used to annotate the Murray cod genome, leading to the identification of 26 539 protein-coding genes. We present the whole genome of the Murray cod and anticipate this will be a catalyst for a range of genetic, genomic, and phylogenetic studies of the Murray cod and more generally other fish species of the Percichthydae family.

31 October 2013 in Microbiology Resource Announcements
Verified
Journal Article
Open access
PDF file
VRVellaya Rehvathy
Vellaya Rehvathy
MTMun Hua Tan
Mun Hua Tan
SGSelva Perumal Gunaletchumy
Selva Perumal Gunaletchumy
XTXinsheng Teh
Xinsheng Teh
SWSusana Wang
Susana Wang
KVKumutha Malar Vellasamy
Kumutha Malar Vellasamy
Helicobacter pylori causes human gastroduodenal diseases, including chronic gastritis and peptic ulcer disease. It is also a major microbial risk factor for the development of gastric adenocarcinoma and mucosa-associated lymphoid tissue (MALT) lymphoma. Twenty-one strains with different ethnicity, disease, and antimicrobial susceptibility backgrounds were sequenced by use of Illumina HiSeq and PacBio RS platforms.

11 December 2014 in Scientific Reports
Verified
Journal Article
Open access
SGSelva Perumal Gunaletchumy
Selva Perumal Gunaletchumy
ISIndran Seevasant
Indran Seevasant
MTMun Hua Tan
Mun Hua Tan
LCLarry Croft
Larry Croft
HMHazel M. Mitchell
Hazel M. Mitchell
KVKumutha Malar Vellasamy
Kumutha Malar Vellasamy
Helicobacter pylori infection results in diverse clinical conditions ranging from chronic gastritis and ulceration to gastric adenocarcinoma. Among the multiethnic population of Malaysia, Indians consistently have a higher H. pylori prevalence as compared with Chinese and Malays. Despite the high prevalence of H. pylori, Indians have a relatively low incidence of peptic ulcer disease and gastric cancer. In contrast, gastric cancer and peptic ulcer disease incidence is high in Chinese. H. pylori strains from Chinese strains predominantly belong to the hspEAsia subpopulation while Indian/Malay strains mainly belong to the hspIndia subpopulation. By comparing the genome of 27 Asian strains from different subpopulations, we identified six genes associated with risk of H. pylori-induced peptic ulcer disease and gastric cancer. This study serves as an important foundation for future studies aiming to understand the role of bacterial factors in H. pylori-induced gastro-duodenal diseases.

2 January 2014 in Mitochondrial DNA Part A
Verified
Journal Article
Closed access
PDF file
CAChristopher M. Austin
Christopher M. Austin
MTMun Hua Tan
Mun Hua Tan
LCLarry Croft
Larry Croft
HGHan Ming Gan
Han Ming Gan
The complete mitochondrial genome of Cherax cainii was recovered from partial genome sequencing data using the HiSeq platform. The mitogenome consists of 15,801 base pairs (69% A + T content) containing 13 protein-coding genes, 2 ribosomal subunit genes, 22 transfer RNAs and a 783 bp non-coding AT-rich region. This is the second completely sequenced mitogenome from the genus Cherax after the first reported Cherax destructor mitogenome nearly a decade ago.

2 January 2014 in Mitochondrial DNA
Verified
Journal Article
Closed access
CAChristopher M. Austin
Christopher M. Austin
MTMun Hua Tan
Mun Hua Tan
YLYin Peng Lee
Yin Peng Lee
LCLarry Croft
Larry Croft
MMMark Meekan
Mark Meekan
HGHan Ming Gan
Han Ming Gan
The complete mitochondrial genome of the parasitic copepod Pandarus rhincodonicus was obtained from a partial genome scan using the HiSeq sequencing system. The Pandarus rhincodonicus mitogenome has 14,480 base pairs (62% A+T content) made up of 12 protein-coding genes, 2 ribosomal subunit genes, 22 transfer RNAs, and a putative 384 bp non-coding AT-rich region. This Pandarus mitogenome sequence is the first for the family Pandaridae, the second for the order Siphonostomatoida and the sixth for the Copepoda