Items where Subject is "Genomes Data Processing"
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Acute Myeloid Leukemia
Targeted RNAi of the mitogen-activated protein kinase pathway genes in acute myeloid leukemia cells. Sains Malaysiana, 42 (8). pp. 1131-1137. ISSN 2462-151X (2013)
Acute myeloid leukaemia
Hyperleucocytosis grading score and NPM1 gene mutation among patients with acute myeloid leukemia: Malaysian experience. Springer Nature, 13. pp. 33-40. ISSN 1865-5785 (2020)
Alzheimer’s disease
Allele-specific polymerase chain reaction for the detection of Alzheimer’s disease-related single nucleotide polymorphisms. BMC Medical Genetics, 14 (27). pp. 1-8. ISSN 1471-2350 (2013)
Analysis services
iPROMISE 2018 booklet: accelerating research excellence. [Phamplet] (2018)
Antarctica
Statistical optimisation of phenol degradation and pathway identification through whole genome sequencing of the cold-adapted antarctic bacterium, rhodococcus sp. Strain AQ5-07. International Journal of Molecular Sciences, 21 (24). pp. 1-20. ISSN 1422-0067 (2020)
Array Comparative Genomic Hybridization (aCGH)
Genome-wide analysis of copy number variation identifies candidate gene loci associated with the progression of non-alcoholic fatty liver disease. PLOS ONE, 9 (4). pp. 1-11. ISSN 1932-6203 (2014)
AuNP/SPCE
Clinical performance of reverse transcription loop-mediated isothermal amplification COVID-19 assay on gold-nanoparticle-modified screen-printed carbon electrode using differential pulse voltammetry. Sensors and Materials, 35 (10). pp. 4731-4750. ISSN 2435-0869 (2023)
Bacterial Genomics
iPROMISE 2018 booklet: accelerating research excellence. [Phamplet] (2018)
Body Mass Index (BMI)
Development of PCE-based genotyping method for fat mass obesity-associated (FTO) gene polymorphism rs9939609. Journal of Health and Translational Medicine (JUMMEC), SI (2). pp. 51-54. ISSN 2289-392X (2023)
COVID-19
Clinical performance of reverse transcription loop-mediated isothermal amplification COVID-19 assay on gold-nanoparticle-modified screen-printed carbon electrode using differential pulse voltammetry. Sensors and Materials, 35 (10). pp. 4731-4750. ISSN 2435-0869 (2023)
Cancer-related nsSNPs
Pathogenic nsSNPs that increase the risks of cancers among the Orang Asli and Malays. Scientifc Reports, 11: 16158. pp. 1-22. ISSN 2045-2322 (2021)
Capillary Sequencing
Development of PCE-based genotyping method for fat mass obesity-associated (FTO) gene polymorphism rs9939609. Journal of Health and Translational Medicine (JUMMEC), SI (2). pp. 51-54. ISSN 2289-392X (2023)
Copy number variation (CNV)
A comparison of assays for accurate copy number measurement of the low-affinity fc gamma receptor genes FCGR3A and FCGR3B. PLOS ONE, 10 (1). pp. 1-13. ISSN 1932-6203 (2015)
Genome-wide analysis of copy number variation identifies candidate gene loci associated with the progression of non-alcoholic fatty liver disease. PLOS ONE, 9 (4). pp. 1-11. ISSN 1932-6203 (2014)
De Novo Assembly
Statistical optimisation of phenol degradation and pathway identification through whole genome sequencing of the cold-adapted antarctic bacterium, rhodococcus sp. Strain AQ5-07. International Journal of Molecular Sciences, 21 (24). pp. 1-20. ISSN 1422-0067 (2020)
Double-strand breaks
Meiotic recombination frequencies are affected by nutritional states in saccharomyces cerevisiae. Proceedings of the National Academy of Sciences (PNAS), 98 (25). pp. 14524-14529. ISSN 0027-8424 (2001)
Drug resistance
Diversified lineages and drug-resistance profiles of clinical isolates of Mycobacterium tuberculosis complex in Malaysia. International Journal of Mycobacteriology, 8 (4). pp. 320-328. (2019)
FCGR3 Locus
A comparison of assays for accurate copy number measurement of the low-affinity fc gamma receptor genes FCGR3A and FCGR3B. PLOS ONE, 10 (1). pp. 1-13. ISSN 1932-6203 (2015)
FTO Gene Variant rs9939609
Development of PCE-based genotyping method for fat mass obesity-associated (FTO) gene polymorphism rs9939609. Journal of Health and Translational Medicine (JUMMEC), SI (2). pp. 51-54. ISSN 2289-392X (2023)
Familial Hypercholesterolaemia (FH)
Classifying familial hypercholesterolaemia: a tree-based machine learning approach. International Journal of Advanced Computer Science and Applications, 12 (9). pp. 66-73. ISSN 2156-5570 (2021)
Familial Hypercholesterolemia (FH)
Development of an Optimized Tetra-Amplification Refractory Mutation System PCR for Detection of 12 Pathogenic Familial Hypercholesterolemia Variants in the Asian Population. The Journal of Molecular Diagnostics, 24 (2). pp. 120-130. ISSN 1943-7811 (2022)
Formalin fixed human placenta tissues
Detection of miR-210 in formalin fixed human placental tissues using real time-PCR. Health Scope, 1. pp. 60-64. ISSN 2735-0649 (2020)
Genetic association study
A comparison of assays for accurate copy number measurement of the low-affinity fc gamma receptor genes FCGR3A and FCGR3B. PLOS ONE, 10 (1). pp. 1-13. ISSN 1932-6203 (2015)
Genetic diseases
Development of an Optimized Tetra-Amplification Refractory Mutation System PCR for Detection of 12 Pathogenic Familial Hypercholesterolemia Variants in the Asian Population. The Journal of Molecular Diagnostics, 24 (2). pp. 120-130. ISSN 1943-7811 (2022)
Genetic polymorphism
Allele-specific polymerase chain reaction for the detection of Alzheimer’s disease-related single nucleotide polymorphisms. BMC Medical Genetics, 14 (27). pp. 1-8. ISSN 1471-2350 (2013)
Genetic risk factors
Allele-specific polymerase chain reaction for the detection of Alzheimer’s disease-related single nucleotide polymorphisms. BMC Medical Genetics, 14 (27). pp. 1-8. ISSN 1471-2350 (2013)
Genome
iPROMISE 2018 booklet: accelerating research excellence. [Phamplet] (2018)
Genome-wide analysis
Genome-wide analysis of copy number variation identifies candidate gene loci associated with the progression of non-alcoholic fatty liver disease. PLOS ONE, 9 (4). pp. 1-11. ISSN 1932-6203 (2014)
Genome-wide association studies (GWAS)
Pathogenic nsSNPs that increase the risks of cancers among the Orang Asli and Malays. Scientifc Reports, 11: 16158. pp. 1-22. ISSN 2045-2322 (2021)
Genomewide
Meiotic recombination frequencies are affected by nutritional states in saccharomyces cerevisiae. Proceedings of the National Academy of Sciences (PNAS), 98 (25). pp. 14524-14529. ISSN 0027-8424 (2001)
Genomic DNA
Detection of miR-210 in formalin fixed human placental tissues using real time-PCR. Health Scope, 1. pp. 60-64. ISSN 2735-0649 (2020)
Genomic variants
Analysis of five deep-sequenced trio-genomes of the Peninsular Malaysia Orang Asli and North Borneo populations. BMC Genomics, 20: 842. pp. 1-13. ISSN 1471-2164 (2019)
Genomics
Personalized medicine beyond genomics: new technologies, global health diplomacy and anticipatory governance. Current pharmacogenomics and personalized medicine, 7 (4). pp. 225-230. ISSN 1875-6913 (2009)
Grading score
Hyperleucocytosis grading score and NPM1 gene mutation among patients with acute myeloid leukemia: Malaysian experience. Springer Nature, 13. pp. 33-40. ISSN 1865-5785 (2020)
HA-MRSA Malaysia
The characterization of mecA Gene and SCCmec typing in clinical samples of MRSA. Science Letters, 13 (2). pp. 1-17. ISSN 2682-8626 (2019)
Hepatic fibrosis
Genome-wide analysis of copy number variation identifies candidate gene loci associated with the progression of non-alcoholic fatty liver disease. PLOS ONE, 9 (4). pp. 1-11. ISSN 1932-6203 (2014)
Hyperleucocytosis
Hyperleucocytosis grading score and NPM1 gene mutation among patients with acute myeloid leukemia: Malaysian experience. Springer Nature, 13. pp. 33-40. ISSN 1865-5785 (2020)
Immune Response
Targeted RNAi of the mitogen-activated protein kinase pathway genes in acute myeloid leukemia cells. Sains Malaysiana, 42 (8). pp. 1131-1137. ISSN 2462-151X (2013)
Immune diseases
A comparison of assays for accurate copy number measurement of the low-affinity fc gamma receptor genes FCGR3A and FCGR3B. PLOS ONE, 10 (1). pp. 1-13. ISSN 1932-6203 (2015)
Indigenous populations
Analysis of five deep-sequenced trio-genomes of the Peninsular Malaysia Orang Asli and North Borneo populations. BMC Genomics, 20: 842. pp. 1-13. ISSN 1471-2164 (2019)
Integrative Pharmacogenomics Institute (iPROMISE)
iPROMISE 2018 booklet: accelerating research excellence. [Phamplet] (2018)
Lineage
Diversified lineages and drug-resistance profiles of clinical isolates of Mycobacterium tuberculosis complex in Malaysia. International Journal of Mycobacteriology, 8 (4). pp. 320-328. (2019)
MAPK Pathway
Targeted RNAi of the mitogen-activated protein kinase pathway genes in acute myeloid leukemia cells. Sains Malaysiana, 42 (8). pp. 1131-1137. ISSN 2462-151X (2013)
MRSA
The characterization of mecA Gene and SCCmec typing in clinical samples of MRSA. Science Letters, 13 (2). pp. 1-17. ISSN 2682-8626 (2019)
Machine learning algorithms
Classifying familial hypercholesterolaemia: a tree-based machine learning approach. International Journal of Advanced Computer Science and Applications, 12 (9). pp. 66-73. ISSN 2156-5570 (2021)
Meiotic Recombination
Meiotic recombination frequencies are affected by nutritional states in saccharomyces cerevisiae. Proceedings of the National Academy of Sciences (PNAS), 98 (25). pp. 14524-14529. ISSN 0027-8424 (2001)
Metabolic state
Meiotic recombination frequencies are affected by nutritional states in saccharomyces cerevisiae. Proceedings of the National Academy of Sciences (PNAS), 98 (25). pp. 14524-14529. ISSN 0027-8424 (2001)
MicroRNAs
Detection of miR-210 in formalin fixed human placental tissues using real time-PCR. Health Scope, 1. pp. 60-64. ISSN 2735-0649 (2020)
Multidrug-resistant TB
Diversified lineages and drug-resistance profiles of clinical isolates of Mycobacterium tuberculosis complex in Malaysia. International Journal of Mycobacteriology, 8 (4). pp. 320-328. (2019)
Mutation
Hyperleucocytosis grading score and NPM1 gene mutation among patients with acute myeloid leukemia: Malaysian experience. Springer Nature, 13. pp. 33-40. ISSN 1865-5785 (2020)
Mycobacterium tuberculosis
Diversified lineages and drug-resistance profiles of clinical isolates of Mycobacterium tuberculosis complex in Malaysia. International Journal of Mycobacteriology, 8 (4). pp. 320-328. (2019)
NAFLD (Non-Alcoholic Fatty Liver Disease)
Genome-wide analysis of copy number variation identifies candidate gene loci associated with the progression of non-alcoholic fatty liver disease. PLOS ONE, 9 (4). pp. 1-11. ISSN 1932-6203 (2014)
NPM1 gene
Hyperleucocytosis grading score and NPM1 gene mutation among patients with acute myeloid leukemia: Malaysian experience. Springer Nature, 13. pp. 33-40. ISSN 1865-5785 (2020)
Next-generation Sequencing
Statistical optimisation of phenol degradation and pathway identification through whole genome sequencing of the cold-adapted antarctic bacterium, rhodococcus sp. Strain AQ5-07. International Journal of Molecular Sciences, 21 (24). pp. 1-20. ISSN 1422-0067 (2020)
Obesity
Development of PCE-based genotyping method for fat mass obesity-associated (FTO) gene polymorphism rs9939609. Journal of Health and Translational Medicine (JUMMEC), SI (2). pp. 51-54. ISSN 2289-392X (2023)
Orang Asli and Malays
Pathogenic nsSNPs that increase the risks of cancers among the Orang Asli and Malays. Scientifc Reports, 11: 16158. pp. 1-22. ISSN 2045-2322 (2021)
Paralogue ratio test-restriction enzyme digest variant ratio (PRT-REDVR)
A comparison of assays for accurate copy number measurement of the low-affinity fc gamma receptor genes FCGR3A and FCGR3B. PLOS ONE, 10 (1). pp. 1-13. ISSN 1932-6203 (2015)
Pathogenic variants
Pathogenic nsSNPs that increase the risks of cancers among the Orang Asli and Malays. Scientifc Reports, 11: 16158. pp. 1-22. ISSN 2045-2322 (2021)
Development of an Optimized Tetra-Amplification Refractory Mutation System PCR for Detection of 12 Pathogenic Familial Hypercholesterolemia Variants in the Asian Population. The Journal of Molecular Diagnostics, 24 (2). pp. 120-130. ISSN 1943-7811 (2022)
Pharmacogenetic
Personalized medicine beyond genomics: new technologies, global health diplomacy and anticipatory governance. Current pharmacogenomics and personalized medicine, 7 (4). pp. 225-230. ISSN 1875-6913 (2009)
Polymerase chain reaction (PCR)
Allele-specific polymerase chain reaction for the detection of Alzheimer’s disease-related single nucleotide polymorphisms. BMC Medical Genetics, 14 (27). pp. 1-8. ISSN 1471-2350 (2013)
Population diversity
Analysis of five deep-sequenced trio-genomes of the Peninsular Malaysia Orang Asli and North Borneo populations. BMC Genomics, 20: 842. pp. 1-13. ISSN 1471-2164 (2019)
Precision health
iPROMISE 2018 booklet: accelerating research excellence. [Phamplet] (2018)
Predicting FH
Classifying familial hypercholesterolaemia: a tree-based machine learning approach. International Journal of Advanced Computer Science and Applications, 12 (9). pp. 66-73. ISSN 2156-5570 (2021)
Primary Health Care
Personalized medicine beyond genomics: new technologies, global health diplomacy and anticipatory governance. Current pharmacogenomics and personalized medicine, 7 (4). pp. 225-230. ISSN 1875-6913 (2009)
RNA Interference
Targeted RNAi of the mitogen-activated protein kinase pathway genes in acute myeloid leukemia cells. Sains Malaysiana, 42 (8). pp. 1131-1137. ISSN 2462-151X (2013)
RT-LAMP
Clinical performance of reverse transcription loop-mediated isothermal amplification COVID-19 assay on gold-nanoparticle-modified screen-printed carbon electrode using differential pulse voltammetry. Sensors and Materials, 35 (10). pp. 4731-4750. ISSN 2435-0869 (2023)
RT-PCR
Detection of miR-210 in formalin fixed human placental tissues using real time-PCR. Health Scope, 1. pp. 60-64. ISSN 2735-0649 (2020)
Clinical performance of reverse transcription loop-mediated isothermal amplification COVID-19 assay on gold-nanoparticle-modified screen-printed carbon electrode using differential pulse voltammetry. Sensors and Materials, 35 (10). pp. 4731-4750. ISSN 2435-0869 (2023)
Rhodococcus
Statistical optimisation of phenol degradation and pathway identification through whole genome sequencing of the cold-adapted antarctic bacterium, rhodococcus sp. Strain AQ5-07. International Journal of Molecular Sciences, 21 (24). pp. 1-20. ISSN 1422-0067 (2020)
SCCmec type
The characterization of mecA Gene and SCCmec typing in clinical samples of MRSA. Science Letters, 13 (2). pp. 1-17. ISSN 2682-8626 (2019)
Saccharomyces Derevisiae
Meiotic recombination frequencies are affected by nutritional states in saccharomyces cerevisiae. Proceedings of the National Academy of Sciences (PNAS), 98 (25). pp. 14524-14529. ISSN 0027-8424 (2001)
Sequenom MassARRAY
A comparison of assays for accurate copy number measurement of the low-affinity fc gamma receptor genes FCGR3A and FCGR3B. PLOS ONE, 10 (1). pp. 1-13. ISSN 1932-6203 (2015)
Single Nucleotide Polymorphisms (SNP)
Pathogenic nsSNPs that increase the risks of cancers among the Orang Asli and Malays. Scientifc Reports, 11: 16158. pp. 1-22. ISSN 2045-2322 (2021)
Single nucleotide polymorphism
Allele-specific polymerase chain reaction for the detection of Alzheimer’s disease-related single nucleotide polymorphisms. BMC Medical Genetics, 14 (27). pp. 1-8. ISSN 1471-2350 (2013)
Staphylococcus aureus
The characterization of mecA Gene and SCCmec typing in clinical samples of MRSA. Science Letters, 13 (2). pp. 1-17. ISSN 2682-8626 (2019)
Tetra-amplification mutation system (T-ARMS)
Development of an Optimized Tetra-Amplification Refractory Mutation System PCR for Detection of 12 Pathogenic Familial Hypercholesterolemia Variants in the Asian Population. The Journal of Molecular Diagnostics, 24 (2). pp. 120-130. ISSN 1943-7811 (2022)
Theragnostics
Personalized medicine beyond genomics: new technologies, global health diplomacy and anticipatory governance. Current pharmacogenomics and personalized medicine, 7 (4). pp. 225-230. ISSN 1875-6913 (2009)
Transcription factor Gcn4p
Meiotic recombination frequencies are affected by nutritional states in saccharomyces cerevisiae. Proceedings of the National Academy of Sciences (PNAS), 98 (25). pp. 14524-14529. ISSN 0027-8424 (2001)
Tree-based classifier
Classifying familial hypercholesterolaemia: a tree-based machine learning approach. International Journal of Advanced Computer Science and Applications, 12 (9). pp. 66-73. ISSN 2156-5570 (2021)
Whole-genome deep sequencing
Analysis of five deep-sequenced trio-genomes of the Peninsular Malaysia Orang Asli and North Borneo populations. BMC Genomics, 20: 842. pp. 1-13. ISSN 1471-2164 (2019)
Whole-genome sequencing
Diversified lineages and drug-resistance profiles of clinical isolates of Mycobacterium tuberculosis complex in Malaysia. International Journal of Mycobacteriology, 8 (4). pp. 320-328. (2019)
differential pulse voltammetry
Clinical performance of reverse transcription loop-mediated isothermal amplification COVID-19 assay on gold-nanoparticle-modified screen-printed carbon electrode using differential pulse voltammetry. Sensors and Materials, 35 (10). pp. 4731-4750. ISSN 2435-0869 (2023)
electrochemical sensor
Clinical performance of reverse transcription loop-mediated isothermal amplification COVID-19 assay on gold-nanoparticle-modified screen-printed carbon electrode using differential pulse voltammetry. Sensors and Materials, 35 (10). pp. 4731-4750. ISSN 2435-0869 (2023)
mecA gene
The characterization of mecA Gene and SCCmec typing in clinical samples of MRSA. Science Letters, 13 (2). pp. 1-17. ISSN 2682-8626 (2019)
miR-210
Detection of miR-210 in formalin fixed human placental tissues using real time-PCR. Health Scope, 1. pp. 60-64. ISSN 2735-0649 (2020)
β-keto-adipate Pathway
Statistical optimisation of phenol degradation and pathway identification through whole genome sequencing of the cold-adapted antarctic bacterium, rhodococcus sp. Strain AQ5-07. International Journal of Molecular Sciences, 21 (24). pp. 1-20. ISSN 1422-0067 (2020)