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index medicus (15) 15
humans (14) 14
mutation (13) 13
multidisciplinary sciences (11) 11
pancreatic neoplasms - genetics (9) 9
genomes (7) 7
genomics (7) 7
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cancer (6) 6
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genes (6) 6
genetic aspects (6) 6
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dna mutational analysis (5) 5
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gene expression (4) 4
gene expression regulation, neoplastic (4) 4
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physiological aspects (4) 4
adenocarcinoma - genetics (3) 3
base sequence (3) 3
carcinoma, pancreatic ductal - pathology (3) 3
cell line, tumor (3) 3
deoxyribonucleic acid--dna (3) 3
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instability (3) 3
medicine (3) 3
metastasis (3) 3
methods (3) 3
methylation (3) 3
molecular sequence data (3) 3
mutation - genetics (3) 3
pancreatic neoplasms - metabolism (3) 3
pancreatic neoplasms - pathology (3) 3
patients (3) 3
research article (3) 3
science (3) 3
signatures (3) 3
transcriptome (3) 3
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analysis (2) 2
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brain (2) 2
cancer genetics (2) 2
carcinoma (2) 2
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chromosome aberrations (2) 2
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chromothripsis (2) 2
computational biology (2) 2
copy number (2) 2
copy-number alteration (2) 2
deoxyribonucleic acid (2) 2
discovery (2) 2
dna (2) 2
dna copy number variations - genetics (2) 2
dna repair - genetics (2) 2
ductal adenocarcinoma (2) 2
gene amplification (2) 2
gene dosage (2) 2
gene expression profiling - methods (2) 2
genes, brca1 (2) 2
genes, brca2 (2) 2
genetics (2) 2
germ-line mutation - genetics (2) 2
high-throughput nucleotide sequencing - methods (2) 2
male (2) 2
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nucleotide sequencing (2) 2
pancreatic neoplasms - classification (2) 2
pathology (2) 2
patterns (2) 2
point mutation - genetics (2) 2
polymerase chain reaction - methods (2) 2
polymorphism, single nucleotide (2) 2
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rna (2) 2
rna sequencing (2) 2
sequence analysis, dna (2) 2
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single-nucleotide polymorphism (2) 2
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1. Full Text Genomic analyses identify molecular subtypes of pancreatic cancer
by Bailey, Peter and Chang, David K and Nones, Katia and Johns, Amber L and Patch, Ann-Marie and Gingras, Marie-Claude and Miller, David K and Christ, Angelika N and Bruxner, Tim J. C and Quinn, Michael C and Nourse, Craig and Murtaugh, L. Charles and Harliwong, Ivon and Idrisoglu, Senel and Manning, Suzanne and Nourbakhsh, Ehsan and Wani, Shivangi and Fink, Lynn and Holmes, Oliver and Chin, Venessa and Anderson, Matthew J and Kazakoff, Stephen and Leonard, Conrad and Newell, Felicity and Waddell, Nick and Wood, Scott and Xu, Qinying and Wilson, Peter J and Cloonan, Nicole and Kassahn, Karin S and Taylor, Darrin and Quek, Kelly and Robertson, Alan and Pantano, Lorena and Mincarelli, Laura and Sanchez, Luis N and Evers, Lisa and Wu, Jianmin and Pinese, Mark and Cowley, Mark J and Jones, Marc D and Colvin, Emily K and Nagrial, Adnan M and Humphrey, Emily S and Chantrill, Lorraine A and Mawson, Amanda and Humphris, Jeremy and Chou, Angela and Pajic, Marina and Scarlett, Christopher J and Pinho, Andreia V and Giry-Laterriere, Marc and Rooman, Ilse and Samra, Jaswinder S and Kench, James G and Lovell, Jessica A and Merrett, Neil D and Toon, Christopher W and Epari, Krishna and Nguyen, Nam Q and Barbour, Andrew and Zeps, Nikolajs and Moran-Jones, Kim and Jamieson, Nigel B and Graham, Janet S and Duthie, Fraser and Oien, Karin and Hair, Jane and Grützmann, Robert and Maitra, Anirban and Iacobuzio-Donahue, Christine A and Wolfgang, Christopher L and Morgan, Richard A and Lawlor, Rita T and Corbo, Vincenzo and Bassi, Claudio and Rusev, Borislav and Capelli, Paola and Salvia, Roberto and Tortora, Giampaolo and Mukhopadhyay, Debabrata and Petersen, Gloria M and Munzy, Donna M and Fisher, William E and Karim, Saadia A and Eshleman, James R and Hruban, Ralph H and Pilarsky, Christian and Morton, Jennifer P and Sansom, Owen J and Scarpa, Aldo and Musgrove, Elizabeth A and Bailey, Ulla-Maja Hagbo and Hofmann, Oliver and Sutherland, Robert L and Wheeler, David A and Gill, Anthony J and Gibbs, Richard A and Pearson, John V and Waddell, Nicola and ... and Australian Pancreatic Canc Genome and Australian Pancreatic Cancer Genome Initiative
Nature, ISSN 0028-0836, 03/2016, Volume 531, Issue 7592, pp. 47 - 52
Integrated genomic analysis of 456 pancreatic ductal adenocarcinomas identified 32 recurrently mutated genes that aggregate into 10 pathways: KRAS, TGF-beta,... 
PATHWAYS | METASTASIS | DUCTAL ADENOCARCINOMA | PACKAGE | MULTIDISCIPLINARY SCIENCES | TUMOR | MUTATIONS | DIFFERENTIATION | Pancreatic Neoplasms - metabolism | Prognosis | Hepatocyte Nuclear Factor 3-beta - genetics | Genomics | Humans | Carcinoma, Pancreatic Ductal - metabolism | Gene Expression Regulation, Neoplastic | Transcriptome | Hepatocyte Nuclear Factor 3-gamma - genetics | Gene Regulatory Networks | Histone Demethylases - genetics | Tumor Suppressor Protein p53 - genetics | Carcinoma, Pancreatic Ductal - genetics | DNA Methylation | Tumor Suppressor Proteins - genetics | Carcinoma, Pancreatic Ductal - classification | Trans-Activators - genetics | Pancreatic Neoplasms - classification | Transcription, Genetic | Nuclear Proteins - genetics | Carcinoma, Pancreatic Ductal - immunology | Genes, Neoplasm - genetics | Basic Helix-Loop-Helix Transcription Factors - genetics | Pancreatic Neoplasms - pathology | Pancreatic Neoplasms - genetics | Receptors, Cytoplasmic and Nuclear - genetics | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Mutation - genetics | Carcinoma, Pancreatic Ductal - pathology | Genome, Human - genetics | Homeodomain Proteins - genetics | Animals | Pancreatic Neoplasms - immunology | Survival Analysis | Cell Line, Tumor | Mice | Physiological aspects | Pancreatic cancer | Methods | Genes | Genomes | Mutation | Gene expression | Tumors
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2. Full Text Whole genomes redefine the mutational landscape of pancreatic cancer
by Waddell, Nicola and Pajic, Marina and Patch, Ann-Marie and Chang, David K and Kassahn, Karin S and Bailey, Peter and Johns, Amber L and Miller, David and Nones, Katia and Quek, Kelly and Quinn, Michael C. J and Robertson, Alan J and Fadlullah, Muhammad Z. H and Bruxner, Tim J. C and Christ, Angelika N and Harliwong, Ivon and Idrisoglu, Senel and Manning, Suzanne and Nourse, Craig and Nourbakhsh, Ehsan and Wani, Shivangi and Wilson, Peter J and Markham, Emma and Cloonan, Nicole and Anderson, Matthew J and Fink, J. Lynn and Holmes, Oliver and Kazakoff, Stephen H and Leonard, Conrad and Newell, Felicity and Poudel, Barsha and Song, Sarah and Taylor, Darrin and Waddell, Nick and Wood, Scott and Xu, Qinying and Wu, Jianmin and Pinese, Mark and Cowley, Mark J and Lee, Hong C and Jones, Marc D and Nagrial, Adnan M and Humphris, Jeremy and Chantrill, Lorraine A and Chin, Venessa and Steinmann, Angela M and Mawson, Amanda and Humphrey, Emily S and Colvin, Emily K and Chou, Angela and Scarlett, Christopher J and Pinho, Andreia V and Giry-Laterriere, Marc and Rooman, Ilse and Samra, Jaswinder S and Kench, James G and Pettitt, Jessica A and Merrett, Neil D and Toon, Christopher and Epari, Krishna and Nguyen, Nam Q and Barbour, Andrew and Zeps, Nikolajs and Jamieson, Nigel B and Graham, Janet S and Niclou, Simone P and Bjerkvig, Rolf and Grützmann, Robert and Aust, Daniela and Hruban, Ralph H and Maitra, Anirban and Iacobuzio-Donahue, Christine A and Wolfgang, Christopher L and Morgan, Richard A and Lawlor, Rita T and Corbo, Vincenzo and Bassi, Claudio and Falconi, Massimo and Zamboni, Giuseppe and Tortora, Giampaolo and Tempero, Margaret A and Gill, Anthony J and Eshleman, James R and Pilarsky, Christian and Scarpa, Aldo and Musgrove, Elizabeth A and Pearson, John V and Biankin, Andrew V and Grimmond, Sean M and Australian Pancreatic Canc Genome and Australian Pancreatic Cancer Genome Initiative
Nature, ISSN 0028-0836, 02/2015, Volume 518, Issue 7540, pp. 495 - 501
Pancreatic cancer remains one of the most lethal of malignancies and a major health burden. We performed whole-genome sequencing and copy number variation... 
REARRANGEMENT | INSTABILITY | METAANALYSIS | RANDOMIZED-TRIALS | ADENOCARCINOMA | MULTIDISCIPLINARY SCIENCES | GENES | PATTERNS | CHROMOTHRIPSIS | GEMCITABINE | CHEMOTHERAPY | Genomics | Humans | DNA Repair - genetics | Carcinoma, Pancreatic Ductal - genetics | Pancreatic Neoplasms - drug therapy | Point Mutation - genetics | DNA Mutational Analysis | Genes, BRCA2 | Pancreatic Neoplasms - classification | Female | Adenocarcinoma - genetics | Genes, BRCA1 | Platinum - pharmacology | Genomic Instability - genetics | Genotype | Pancreatic Neoplasms - genetics | Mutation - genetics | Adenocarcinoma - drug therapy | Poly(ADP-ribose) Polymerase Inhibitors | Genome, Human - genetics | Xenograft Model Antitumor Assays | Carcinoma, Pancreatic Ductal - drug therapy | Animals | Genetic Markers - genetics | Mice | Copy number variations | Pancreatic cancer | Physiological aspects | Development and progression | Genetic aspects | Research | Tumor proteins | Risk factors | Genes | DNA damage | Clinical trials | Genomes | Cancer therapies | Patients | Biomarkers | Mutation | Chromosomes | Deoxyribonucleic acid--DNA | Tumors
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3. Full Text Whole-genome characterization of chemoresistant ovarian cancer
by Patch, Ann-Marie and Christie, Elizabeth L and Etemadmoghadam, Dariush and Garsed, Dale W and George, Joshy and Fereday, Sian and Nones, Katia and Cowin, Prue and Alsop, Kathryn and Bailey, Peter J and Kassahn, Karin S and Newell, Felicity and Quinn, Michael C.J and Kazakoff, Stephen and Quek, Kelly and Wilhelm-Benartzi, Charlotte and Curry, Ed and Leong, Huei San and Hamilton, Anne and Mileshkin, Linda and Au-Yeung, George and Kennedy, Catherine and Hung, Jillian and Chiew, Yoke-Eng and Harnett, Paul and Friedlander, Michael and Quinn, Michael and Pyman, Jan and Cordner, Stephen and O'Brien, Patricia and Leditschke, Jodie and Young, Greg and Strachan, Kate and Waring, Paul and Azar, Walid and Mitchell, Chris and Traficante, Nadia and Hendley, Joy and Thorne, Heather and Shackleton, Mark and Miller, David K and Arnau, Gisela Mir and Tothill, Richard W and Holloway, Timothy P and Semple, Timothy and Harliwong, Ivon and Nourse, Craig and Nourbakhsh, Ehsan and Manning, Suzanne and Idrisoglu, Senel and Bruxner, Timothy J. C and Christ, Angelika N and Poudel, Barsha and Holmes, Oliver and Anderson, Matthew and Leonard, Conrad and Lonie, Andrew and Hall, Nathan and Wood, Scott and Taylor, Darrin F and Xu, Qinying and Lynn Fink, J and Waddell, Nick and Drapkin, Ronny and Stronach, Euan and Gabra, Hani and Brown, Robert and Jewell, Andrea and Nagaraj, Shivashankar H and Markham, Emma and Wilson, Peter J and Ellul, Jason and McNally, Orla and Doyle, Maria A and Vedururu, Ravikiran and Stewart, Collin and Lengyel, Ernst and Pearson, John V and Waddell, Nicola and Defazio, Anna and Grimmond, Sean M and Bowtell, David D. L and Australian Ovarian Canc Study Grp and Australian Ovarian Cancer Study Group and The Australian Ovarian Cancer Study Group
Nature, ISSN 0028-0836, 05/2015, Volume 521, Issue 7553, pp. 489 - 494
Patients with high-grade serous ovarian cancer (HGSC) have experienced little improvement in overall survival, and standard treatment has not advanced beyond... 
INTERNAL SHOCKS | M87 JET | MUTATIONAL PROCESSES | EVOLUTION | SIGNATURES | MULTIDISCIPLINARY SCIENCES | CLINICAL-TRIALS | BRCA1 | COPY-NUMBER ALTERATION | DISCOVERY | CHEMOTHERAPY RESISTANCE | Oncogene Proteins - genetics | PTEN Phosphohydrolase - genetics | Humans | Mutagenesis - genetics | Cystadenocarcinoma, Serous - genetics | DNA-Binding Proteins - genetics | Genes, Neurofibromatosis 1 | Germ-Line Mutation - genetics | Cyclin E - genetics | Cystadenocarcinoma, Serous - drug therapy | Promoter Regions, Genetic - genetics | Genome, Human - genetics | Ovarian Neoplasms - genetics | DNA Methylation | Drug Resistance, Neoplasm - genetics | ATP-Binding Cassette, Sub-Family B, Member 1 - genetics | DNA Mutational Analysis | Retinoblastoma Protein - genetics | Genes, BRCA2 | Female | Genes, BRCA1 | Ovarian Neoplasms - drug therapy | Cohort Studies | Drug Resistance, Neoplasm - drug effects | Care and treatment | Analysis | Genetic aspects | Nucleotide sequencing | Methylation | Ovarian cancer | DNA sequencing | Gene amplification | Genomes | Mutation | Metastasis | Gene expression | Chromosomes | Patients | Tumors
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4. Full Text Optimized deep-targeted proteotranscriptomic profiling reveals unexplored Conus toxin diversity and novel cysteine frameworks
by Vincent Lavergne and Ivon Harliwong and Alun Jones and David Miller and Ryan J. Taft and Paul F. Alewood
Proceedings of the National Academy of Sciences, ISSN 0027-8424, 07/2015, Volume 112, Issue 29, pp. E3782 - E3791
Cone snails are predatory marine gastropods characterized by a sophisticated venom apparatus responsible for the biosynthesis and delivery of complex mixtures... 
Bioinformatic | Conotoxin | Transcriptomic | Cysteine-rich peptides | Proteomic | GENE SUPERFAMILY | transcriptomic | MULTIDISCIPLINARY SCIENCES | proteomic | bioinformatic | RIBOSOMAL-RNA | MOLECULAR PHYLOGENY | CONOTOXIN SUPERFAMILY | MASS-SPECTROMETRY | conotoxin | GEOGRAPHUS VENOM | MARINE GASTROPOD | REFERENCE GENOME | VENOM-DUCT TRANSCRIPTOME | cysteine-rich peptides | RNA-SEQ DATA | Multigene Family | RNA Editing | DNA, Complementary - genetics | Peptides - genetics | Molecular Sequence Data | Conus Snail - anatomy & histology | Gene Expression Profiling | Chromatography, High Pressure Liquid | RNA - genetics | Chromatography, Reverse-Phase | Peptides - metabolism | Cysteine - metabolism | Codon - genetics | RNA - metabolism | Amino Acid Sequence | Gene Library | Peptides - chemistry | Conotoxins - genetics | Conotoxins - metabolism | Sequence Analysis, DNA | Amino Acid Motifs | Conotoxins - chemistry | Conus Snail - chemistry | Sequence Alignment | Animals | Chemical Fractionation | Proteomics | Animal Structures - metabolism | Cysteine | Genetic aspects | Research | Marine toxins | Health aspects | Cone snails | Amino acids | Mollusks | Biosynthesis | Toxins | Peptides | Venom | Biological Sciences | PNAS Plus
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5. Full Text Whole-genome landscape of pancreatic neuroendocrine tumours
by Scarpa, Aldo and Chang, David K and Nones, Katia and Corbo, Vincenzo and Patch, Ann-Marie and Bailey, Peter and Lawlor, Rita T and Johns, Amber L and Miller, David K and Mafficini, Andrea and Rusev, Borislav and Scardoni, Maria and Antonello, Davide and Barbi, Stefano and Sikora, Katarzyna O and Cingarlini, Sara and Vicentini, Caterina and McKay, Skye and Quinn, Michael C.J and Bruxner, Timothy J.C and Christ, Angelika N and Harliwong, Ivon and Idrisoglu, Senel and McLean, Suzanne and Nourse, Craig and Nourbakhsh, Ehsan and Wilson, Peter J and Anderson, Matthew J and Fink, J. Lynn and Newell, Felicity and Waddell, Nick and Holmes, Oliver and Kazakoff, Stephen H and Leonard, Conrad and Wood, Scott and Xu, Qinying and Nagaraj, Shivashankar Hiriyur and Amato, Eliana and Dalai, Irene and Bersani, Samantha and Cataldo, Ivana and Dei Tos, Angelo P and Capelli, Paola and Davì, Maria Vittoria and Landoni, Luca and Malpaga, Anna and Miotto, Marco and Whitehall, Vicki L.J and Leggett, Barbara A and Harris, Janelle L and Harris, Jonathan and Jones, Marc D and Humphris, Jeremy and Chantrill, Lorraine A and Chin, Venessa and Nagrial, Adnan M and Pajic, Marina and Scarlett, Christopher J and Pinho, Andreia and Rooman, Ilse and Toon, Christopher and Wu, Jianmin and Pinese, Mark and Cowley, Mark and Barbour, Andrew and Mawson, Amanda and Humphrey, Emily S and Colvin, Emily K and Chou, Angela and Lovell, Jessica A and Jamieson, Nigel B and Duthie, Fraser and Gingras, Marie-Claude and Fisher, William E and Dagg, Rebecca A and Lau, Loretta M.S and Lee, Michael and Pickett, Hilda A and Reddel, Roger R and Samra, Jaswinder S and Kench, James G and Merrett, Neil D and Epari, Krishna and Nguyen, Nam Q and Zeps, Nikolajs and Falconi, Massimo and Simbolo, Michele and Butturini, Giovanni and Van Buren, George and Partelli, Stefano and Fassan, Matteo and Khanna, Kum Kum and Gill, Anthony J and Wheeler, David A and Gibbs, Richard A and Musgrove, Elizabeth A and Bassi, Claudio and Tortora, Giampaolo and Pederzoli, Paolo and Pearson, John V and ... and Australian Pancreatic Canc Genome and Australian Pancreatic Cancer Genome Initiative
Nature, ISSN 0028-0836, 03/2017, Volume 543, Issue 7643, pp. 65 - 71
The diagnosis of pancreatic neuroendocrine tumours (PanNETs) is increasing owing to more sensitive detection methods, and this increase is creating challenges... 
MOLECULAR SUBTYPES | MUTATIONAL PROCESSES | TRANSLOCATION | SUPPRESSOR | PROTEIN | PATHWAY GENES | MULTIDISCIPLINARY SCIENCES | MTOR PATHWAY | TP53 MUTATIONS | CANCER | EWING SARCOMA | Calmodulin-Binding Proteins - genetics | RNA-Binding Proteins - genetics | TOR Serine-Threonine Kinases - metabolism | Genomics | Humans | DNA Glycosylases - genetics | Carcinoma, Neuroendocrine - genetics | Chromatin Assembly and Disassembly - genetics | Male | Pancreatic Neoplasms - genetics | DNA Copy Number Variations - genetics | DNA Repair - genetics | Germ-Line Mutation - genetics | Genome, Human - genetics | DNA Mutational Analysis | Base Sequence | Chromosome Aberrations | Female | Telomere - metabolism | RNA-Binding Protein EWS | Telomere - genetics | Genetic aspects | Nucleotide sequencing | Pancreatic cancer | Methods | DNA sequencing | Genes | Biomarkers | Genomes | Mutation | Signatures | Patients | Tumors | Index Medicus
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6. Full Text Genomic catastrophes frequently arise in esophageal adenocarcinoma and drive tumorigenesis
by Nones, Katia and Waddell, Nicola and Wayte, Nicci and Patch, Ann-Marie and Bailey, Peter and Newell, Felicity and Holmes, Oliver and Fink, J. Lynn and Quinn, Michael C. J and Tang, Yue Hang and Lampe, Guy and Quek, Kelly and Loffler, Kelly A and Manning, Suzanne and Idrisoglu, Senel and Miller, David and Xu, Qinying and Waddell, Nick and Wilson, Peter J and Bruxner, Timothy J. C and Christ, Angelika N and Harliwong, Ivon and Nourse, Craig and Nourbakhsh, Ehsan and Anderson, Matthew and Kazakoff, Stephen and Leonard, Conrad and Wood, Scott and Simpson, Peter T and Reid, Lynne E and Krause, Lutz and Hussey, Damian J and Watson, David I and Lord, Reginald V and Nancarrow, Derek and Phillips, Wayne A and Gotley, David and Smithers, B. Mark and Whiteman, David C and Hayward, Nicholas K and Campbell, Peter J and Pearson, John V and Grimmond, Sean M and Barbour, Andrew P
Nature Communications, ISSN 2041-1723, 2014, Volume 5, Issue 1, p. 5224
Oesophageal adenocarcinoma (EAC) incidence is rapidly increasing in Western countries. A better understanding of EAC underpins efforts to improve early... 
REARRANGEMENT | MUTATIONAL PROCESSES | INSTABILITY | MULTIDISCIPLINARY SCIENCES | IN-VIVO | PATTERNS | BARRETTS-ESOPHAGUS | COPY-NUMBER ALTERATION | CHROMOTHRIPSIS | CANCER GENOMES | Carcinogenesis - pathology | Adenocarcinoma - pathology | Esophageal Neoplasms - genetics | Chromosomes, Human - genetics | Humans | Carcinogenesis - genetics | Adenocarcinoma - genetics | Gene Rearrangement - genetics | Mutation - genetics | Chromosome Breakage | Genome, Human - genetics | Esophageal Neoplasms - pathology
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7. Full Text Optimized deep-targeted proteotranscriptomic profiling reveals unexploredConustoxin diversity and novel cysteine frameworks
by Vincent Lavergne and Ivon Harliwong and Alun Jones and David Miller and Ryan J. Taft and Paul F. Alewood
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 7/2015, Volume 112, Issue 29, pp. E3782 - E3791
Cone snails are predatory marine gastropods characterized by a sophisticated venom apparatus responsible for the biosynthesis and delivery of complex mixtures... 
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8. Full Text qpure: A Tool to Estimate Tumor Cellularity from Genome-Wide Single-Nucleotide Polymorphism Profiles
by Song, Sarah and Nones, Katia and Miller, David and Harliwong, Ivon and Kassahn, Karin S and Pinese, Mark and Pajic, Marina and Gill, Anthony J and Johns, Amber L and Anderson, Matthew and Holmes, Oliver and Leonard, Conrad and Taylor, Darrin and Wood, Scott and Xu, Qinying and Newell, Felicity and Cowley, Mark J and Wu, Jianmin and Wilson, Peter and Fink, Lynn and Biankin, Andrew V and Waddell, Nic and Grimmond, Sean M and Pearson, John V
PLoS ONE, ISSN 1932-6203, 09/2012, Volume 7, Issue 9, p. e45835
Tumour cellularity, the relative proportion of tumour and normal cells in a sample, affects the sensitivity of mutation detection, copy number analysis, cancer... 
MUTATION DETECTION | MULTIDISCIPLINARY SCIENCES | SAMPLES | Computational Biology - methods | Genome-Wide Association Study | Pancreatic Neoplasms - metabolism | Exons | Gene Frequency | Humans | Gene Expression Regulation | Pancreatic Neoplasms - genetics | Models, Statistical | Loss of Heterozygosity | Sequence Analysis, DNA | Regression Analysis | Algorithms | Cell Line, Tumor | Models, Genetic | Polymorphism, Single Nucleotide | Software | Mutation | Physiological aspects | Genetic aspects | Research | Single nucleotide polymorphisms | Tumors | Correlation | Parameter estimation | Copy number | Genomics | Genomes | Statistical methods | Single-nucleotide polymorphism | Experiments | K-Ras protein | DNA methylation | Mathematical models | Lesions | Deoxyribonucleic acid--DNA | Medical research | Discriminant analysis | Sensitivity analysis | Statistical analysis | Gene expression | Estimates | Heterozygosity | Pathology | Reviews | Gene frequency | Pancreatic cancer | Loss of heterozygosity | Genetic testing | Methylation | Cancer | Polymorphism | Deoxyribonucleic acid | DNA
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