-
pubmed
Mandola AB, Frizinsky S, Somekh I, Naor S 等
2026 Aug
置信度 0.82
-
pubmed
Conforti S, Kapopoulou A, Bank C, Köchle B 等
2026
置信度 0.82
-
pubmed
Xiong J, Shang M, Bao J, Liu T 等
2026 Aug 6
置信度 0.82
-
pubmed
Ke L, Cecchini M, Townsend JP
2026 Aug 5
置信度 0.82
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pubmed
Zhang Y, Zhang T, Yin Q, Luo H
2026 Aug 5
置信度 0.82
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pubmed
Ran C, Deborgies Sanches C, Swedblom J, Wellfelt K 等
2026 Aug 4
置信度 0.82
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pubmed
Yay A, Gonen ZB, Kalkan KT, Yalcın B 等
2026 Aug 5
置信度 0.82
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pubmed
Basu M
2026 Aug 5
置信度 0.82
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pubmed
2026 Aug 5
置信度 0.82
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pubmed
Park RF, Chhetri M, Sandhu KS, Ziems L 等
2026 Aug 5
置信度 0.82
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pubmed
Hensley PJ, Teoh JYC, Li R, Gupta S 等
2026 Aug 5
置信度 0.82
-
pubmed
Bersch-Ferreira AC, Santos RHN, Rogero MM, Machado RHV 等
2026 Aug 5
置信度 0.82
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pubmed
McKenzie J, Howard L, Park JJ, Ashraf B 等
2026 Aug 5
置信度 0.82
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pubmed
Kim JS, Uppalapati S, Margolis A, McClelland M 等
2026 Aug 5
置信度 0.82
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pubmed
Letebo A, Vanheer LN, Engdaw M, Ejigu LA 等
2026 Aug 5
置信度 0.82
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pubmed
Dutta P, Pagnamenta AT, Robert C, McGuigan AEF 等
2026 Aug 5
置信度 0.82
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pubmed
Assamad D, Saeedi S, Grewal S, Jha V 等
2026 Aug 5
置信度 0.82
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pubmed
Zhu S, Tang H, Jones T, Fumia N 等
2026 Aug 5
置信度 0.82
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pubmed
Moore H, Dehnad M, Freelin A, Granger B 等
2026 Aug 5
置信度 0.82
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pubmed
Poh AR, Sexton A, Pietrzak H, De Losa R 等
2026 Aug 3
置信度 0.82
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pubmed
Vasileva DP, Chhetri HB, Hochanadel LH, Streich JC 等
2026 Aug 5
置信度 0.82
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pubmed
Loginova M, Morozova N, Paramonov I
2026 Aug
置信度 0.82
-
pubmed
RenChen X, Wu B, Dang Z
2026 Aug 17
置信度 0.82
-
pubmed
Jhou DW, Yang CY, Lao CK, Chen NY 等
2026 Aug 4
置信度 0.82
-
pubmed
Sparks JA
2026 Aug 5
置信度 0.82
-
pubmed
Shu F, Wang Z, Chen W, Liu M
2026 Aug 5
置信度 0.82
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pubmed
Davis JM, Norwitz ER
2026 Sep
置信度 0.82
-
pubmed
Pawloski KR, Barrio AV
2026 Sep
置信度 0.82
-
Here, we present a major advance of the OrthoFinder method. This extends OrthoFinder's high accuracy orthogroup inference to provide phylogenetic inference of orthologs, rooted gene trees, gene duplication events, the rooted species tree, and comparative genom…
openalex
David Emms, Steven Kelly
2019-11-14
置信度 0.72
InferencePhylogenetic treeBiologyGenomicsComputational biology
-
A catalogue of molecular aberrations that cause ovarian cancer is critical for developing and deploying therapies that will improve patients’ lives. The Cancer Genome Atlas project has analysed messenger RNA expression, microRNA expression, promoter methylatio…
openalex
Debra Bell, Andrew Berchuck, Michael J. Birrer, Marcin Imieliński 等
2011-06-28
置信度 0.72
Ovarian cancerBiologymicroRNADNA methylationExon
-
Efficient methods for processing genomic data were developed to increase reliability of estimated breeding values and to estimate thousands of marker effects simultaneously. Algorithms were derived and computer programs tested with simulated data for 2,967 bul…
openalex
P.M. VanRaden
2008-10-22
置信度 0.72
Linkage disequilibriumGenomic selectionStatisticsLinkage (software)Selection (genetic algorithm)
-
The UK Biobank project is a prospective cohort study with deep genetic and phenotypic data collected on approximately 500,000 individuals from across the United Kingdom, aged between 40 and 69 at recruitment. The open resource is unique in its size and scope. …
openalex
Clare Bycroft, Colin Freeman, Desislava Petkova, Gavin Band 等
2018-10-02
置信度 0.72
BiobankImputation (statistics)GenotypeBiologyPopulation
-
We performed an integrated genomic, transcriptomic and proteomic characterization of 373 endometrial carcinomas using array- and sequencing-based technologies. Uterine serous tumours and ∼25% of high-grade endometrioid tumours had extensive copy number alterat…
openalex
Douglas A. Levine
2013-04-30
置信度 0.72
PTENCancer researchSerous fluidBiologyEndometrial cancer
-
openalex
Cameron Brennan, Roel G.W. Verhaak, Aaron McKenna, Benito Campos 等
2013-10-01
置信度 0.72
BiologySomatic cellGlioblastomaGeneticsComputational biology
-
openalex
Roujian Lu, Xiang Zhao, Juan Li, Peihua Niu 等
2020-01-30
置信度 0.72
Phylogenetic treeBiologyCoronavirusVirologySanger sequencing
-
The number of sequenced plant genomes and associated genomic resources is growing rapidly with the advent of both an increased focus on plant genomics from funding agencies, and the application of inexpensive next generation sequencing. To interact with this i…
openalex
David Goodstein, Shengqiang Shu, Russell W. Howson, Rochak Neupane 等
2011-11-22
置信度 0.72
BiologyGenomeGenomicsComparative genomicsFunctional genomics
-
DNA-DNA hybridization (DDH) has been used for nearly 50 years as the gold standard for prokaryotic species circumscriptions at the genomic level. It has been the only taxonomic method that offered a numerical and relatively stable species boundary, and its use…
openalex
Michael Richter, Ramon Rosselló‐Móra
2009-10-23
置信度 0.72
Pairwise comparisonGenomeComputational biologyGenomicsBiology
-
We describe a program, tRNAscan-SE, which identifies 99-100% of transfer RNA genes in DNA sequence while giving less than one false positive per 15 gigabases. Two previously described tRNA detection programs are used as fast, first-pass prefilters to identify …
openalex
Todd M. Lowe, Sean R. Eddy
1997-03-01
置信度 0.72
Transfer RNABiologyGeneticsGeneRNA
-
We describe Bioconductor infrastructure for representing and computing on annotated genomic ranges and integrating genomic data with the statistical computing features of R and its extensions. At the core of the infrastructure are three packages: IRanges, Geno…
openalex
Michael Lawrence, Wolfgang Huber, Hervé Pagès, Patrick Aboyoun 等
2013-08-08
置信度 0.72
BioconductorComputer scienceScalabilitySoftwareVisualization
-
miRBase is the central online repository for microRNA (miRNA) nomenclature, sequence data, annotation and target prediction. The current release (10.0) contains 5071 miRNA loci from 58 species, expressing 5922 distinct mature miRNA sequences: a growth of over …
openalex
Sam Griffiths‐Jones, Harpreet K. Saini, Stijn van Dongen, Anton J. Enright
2007-11-08
置信度 0.72
MiRBaseBiologymicroRNAComputational biologyGenomics
-
Glioblastoma multiforme (GBM) is the most common and lethal type of brain cancer. To identify the genetic alterations in GBMs, we sequenced 20,661 protein coding genes, determined the presence of amplifications and deletions using high-density oligonucleotide …
openalex
D. Williams Parsons, Siân Jones, Xiaosong Zhang, Jimmy Lin 等
2008-09-04
置信度 0.72
IDH1Isocitrate dehydrogenaseGlioblastomaGeneBiology
-
Two new methods were used to establish a rapid and highly sensitive prenatal diagnostic test for sickle cell anemia. The first involves the primer-mediated enzymatic amplification of specific beta-globin target sequences in genomic DNA, resulting in the expone…
openalex
Randall K. Saiki, Stephen J. Scharf, Fred Faloona, Kary B. Mullis 等
1985-12-20
置信度 0.72
Restriction enzymeMolecular biologygenomic DNAEndonucleaseBiology
-
Human cancer cells typically harbour multiple chromosomal aberrations, nucleotide substitutions and epigenetic modifications that drive malignant transformation. The Cancer Genome Atlas (TCGA) pilot project aims to assess the value of large-scale multi-dimensi…
openalex
Roger E. McLendon, D D Bigner, Allan H. Friedman, Erwin G. Van Meir 等
2008-09-04
置信度 0.72
DNA methylationBiologyGeneEpigeneticsCancer
-
The increasing amount of genomic and molecular information is the basis for understanding higher-order biological systems, such as the cell and the organism, and their interactions with the environment, as well as for medical, industrial and other practical ap…
openalex
Minoru Kanehisa
2005-12-28
置信度 0.72
KEGGChemical spaceGenomicsBiologyFunctional genomics
-
As genomes evolve, they undergo large-scale evolutionary processes that present a challenge to sequence comparison not posed by short sequences. Recombination causes frequent genome rearrangements, horizontal transfer introduces new sequences into bacterial ch…
openalex
Aaron E. Darling, Bob Mau, Frederick R. Blattner, Nicole T. Perna
2004-07-01
置信度 0.72
GenomeBiologyComputational biologyLineage (genetic)Genetics
-
BACKGROUND: Recent studies have provided a detailed census of genes that are mutated in acute myeloid leukemia (AML). Our next challenge is to understand how this genetic diversity defines the pathophysiology of AML and informs clinical practice. METHODS: We e…
openalex
Elli Papaemmanuil, Moritz Gerstung, Lars Bullinger, Verena I. Gaidzik 等
2016-06-08
置信度 0.72
NPM1Myeloid leukemiaMedicineMutationGenetics
-
openalex
Roel G.W. Verhaak, Katherine A. Hoadley, Elizabeth Purdom, Victoria Wang 等
2010-01-01
置信度 0.72
PDGFRABiologyIDH1TranscriptomeGene
-
Massively parallel short-read sequencing technologies, coupled with powerful software platforms, are enabling investigators to analyse tens of thousands of genetic markers. This wealth of data is rapidly expanding and allowing biological questions to be addres…
openalex
Julian Catchen, Paul A. Hohenlohe, Susan Bassham, Angel Amores 等
2013-05-24
置信度 0.72
Population genomicsGenomicsBiologyMassively parallelSoftware
-
We explored genomic expression patterns in the yeast Saccharomyces cerevisiae responding to diverse environmental transitions. DNA microarrays were used to measure changes in transcript levels over time for almost every yeast gene, as cells responded to temper…
openalex
Audrey P. Gasch, Paul T. Spellman, Camilla M. Kao, Orna Carmel‐Harel 等
2000-12-01
置信度 0.72
BiologySaccharomyces cerevisiaeYeastGeneGenetics
-
openalex
Mary J. Goldman, Brian Craft, Mim Hastie, Kristupas Repečka 等
2020-05-22
置信度 0.72
GenomicsComputational biologyBiologyData scienceGenome
-
We describe the landscape of genomic alterations in cutaneous melanomas through DNA, RNA, and protein-based analysis of 333 primary and/or metastatic melanomas from 331 patients. We establish a framework for genomic classification into one of four subtypes bas…
openalex
Rehan Akbani, Kadir C. Akdemir, Bülent Arman Aksoy, Monique Albert 等
2015-06-01
置信度 0.72
BiologyMelanomaMutantCancer researchGene
-
openalex
Wolfgang Huber, Vincent J. Carey, Robert Gentleman, Simon Anders 等
2015-01-29
置信度 0.72
BioconductorInteroperabilityComputer scienceSoftwareData science
-
Lung squamous cell carcinoma is a common type of lung cancer, causing approximately 400,000 deaths per year worldwide. Genomic alterations in squamous cell lung cancers have not been comprehensively characterized, and no molecularly targeted agents have been s…
openalex
Peter S. Hammerman, Michael S. Lawrence, Douglas Voet, Rui Jing 等
2012-09-07
置信度 0.72
CDKN2ACancer researchBiologyLung cancerPTEN
-
openalex
Chris Burge, Samuel Karlin
1997-04-01
置信度 0.72
ExonIntronGeneGeneticsBiology
-
A dense set of single nucleotide polymorphisms (SNP) covering the genome and an efficient method to assess SNP genotypes are expected to be available in the near future. An outstanding question is how to use these technologies efficiently to identify genes aff…
openalex
Bernie Devlin, Kathryn Roeder
1999-12-01
置信度 0.72
Bonferroni correctionOutlierFalse positive paradoxSingle-nucleotide polymorphismSNP
-
openalex
METABRIC Group, Christina Curtis, Sohrab P. Shah, Suet‐Feung Chin 等
2012-04-17
置信度 0.72
BiologyTranscriptomeBreast cancerGeneCopy-number variation
-
openalex
Barry S. Taylor, Nikolaus Schultz, Haley Hieronymus, Anuradha Gopalan 等
2010-06-25
置信度 0.72
Prostate cancerChromoplexyBiologyTMPRSS2Prostate
-
In order to extract the maximum amount of information from the rapidly accumulating genome sequences, all conserved genes need to be classified according to their homologous relationships. Comparison of proteins encoded in seven complete genomes from five majo…
openalex
Roman L. Tatusov, Eugene V. Koonin, David J. Lipman
1997-10-24
置信度 0.72
GenomeBiologyPhylogenetic treeGeneticsComputational biology
-
Comparison of DNA sequences from different species is a fundamental method for identifying functional elements in genomes. Here, we describe the VISTA family of tools created to assist biologists in carrying out this task. Our first VISTA server at http://www-…
openalex
Kelly A. Frazer, Lior Pachter, Alexandre Poliakov, Edward M. Rubin 等
2004-07-01
置信度 0.72
BiologyGenomeComparative genomicsGenomicsComputational biology
-
openalex
Peter J. Bailey, David K. Chang, Kátia Nones, Amber L. Johns 等
2016-02-23
置信度 0.72
BiologyPDX1Pancreatic cancerCancer researchKRAS
-
openalex
Steffen Durinck, Paul T. Spellman, Ewan Birney, Wolfgang Huber
2009-07-22
置信度 0.72
EnsemblBioconductorComputer scienceIdentifierComputational biology
-
openalex
Dan R. Robinson, Eliezer M. Van Allen, Yi-Mi Wu, Nikolaus Schultz 等
2015-05-01
置信度 0.72
Prostate cancerBiologyPTENExome sequencingCancer
-
openalex
Igor Ulitsky, David P. Bartel
2013-07-01
置信度 0.72
BiologyGenomicsGenomeComputational biologyVertebrate
-
RepeatMasker is a popular software tool widely used in computational genomics to identify, classify, and mask repetitive elements, including low-complexity sequences and interspersed repeats. RepeatMasker searches for repetitive sequence by aligning the input …
openalex
Maja Tarailo‐Graovac, Nansheng Chen
2009-03-01
置信度 0.72
UnixComputer scienceSequence (biology)SoftwareSequence alignment
-
BACKGROUND: Fluorescence in situ hybridization has improved the detection of genomic aberrations in chronic lymphocytic leukemia. We used this method to identify chromosomal abnormalities in patients with chronic lymphocytic leukemia and assessed their prognos…
openalex
Hartmut Döhner, Stephan Stilgenbauer, Axel Benner, Elke Leupolt 等
2000-12-28
置信度 0.72
Chronic lymphocytic leukemiaTrisomyFluorescence in situ hybridizationComparative genomic hybridizationCytogenetics
-
BACKGROUND: Many mutations that contribute to the pathogenesis of acute myeloid leukemia (AML) are undefined. The relationships between patterns of mutations and epigenetic phenotypes are not yet clear. METHODS: We analyzed the genomes of 200 clinically annota…
openalex
The Cancer Genome Atlas Research Network
2013-05-02
置信度 0.72
EpigenomicsMedicineMyeloid leukemiaMyeloidLeukemia
-
The Cancer Genome Atlas profiled 279 head and neck squamous cell carcinomas (HNSCCs) to provide a comprehensive landscape of somatic genomic alterations. Here we show that human-papillomavirus-associated tumours are dominated by helical domain mutations of the…
openalex
The Cancer Genome Atlas Network
2015-01-27
置信度 0.72
HRASCDKN2ACancer researchBiologyHead and neck squamous-cell carcinoma
-
Papillary thyroid carcinoma (PTC) is the most common type of thyroid cancer. Here, we describe the genomic landscape of 496 PTCs. We observed a low frequency of somatic alterations (relative to other carcinomas) and extended the set of known PTC driver alterat…
openalex
Nishant Agrawal, Rehan Akbani, Bülent Arman Aksoy, Adrian Ally 等
2014-10-01
置信度 0.72
BiologyThyroid carcinomaCancer researchThyroid cancerGene
-
Alterations in cancer genomes strongly influence clinical responses to treatment and in many instances are potent biomarkers for response to drugs. The Genomics of Drug Sensitivity in Cancer (GDSC) database (www.cancerRxgene.org) is the largest public resource…
openalex
Wanjuan Yang, Jorge Soares, Patricia Greninger, Elena J. Edelman 等
2012-11-22
置信度 0.72
BiologyDrug discoveryGenomicsComputational biologyCancer
-
Human cancer is caused by the accumulation of mutations in oncogenes and tumor suppressor genes. To catalog the genetic changes that occur during tumorigenesis, we isolated DNA from 11 breast and 11 colorectal tumors and determined the sequences of the genes i…
openalex
Laura D. Wood, D. Williams Parsons, Siân Jones, Jimmy Lin 等
2007-10-11
置信度 0.72
CarcinogenesisGeneBiologyExonGenomics
-
The accelerating pace of genome sequencing throughout the tree of life is driving the need for improved unsupervised annotation of genome components such as transposable elements (TEs). Because the types and sequences of TEs are highly variable across species,…
openalex
Jullien M. Flynn, Robert Hubley, Clément Goubert, Jeb Rosen 等
2020-04-16
置信度 0.72
AnnotationGenomeTransposable elementComputational biologyBiology
-
DNA microarrays containing virtually every gene of Saccharomyces cerevisiae were used to carry out a comprehensive investigation of the temporal program of gene expression accompanying the metabolic shift from fermentation to respiration. The expression profil…
openalex
Joseph L. DeRisi, Vishwanath R. Iyer, Patrick O. Brown
1997-10-24
置信度 0.72
DNA microarrayYAP1BiologyGeneGene expression
-
openalex
Simona Negrini, Vassilis G. Gorgoulis, Thanos D. Halazonetis
2010-02-23
置信度 0.72
Genome instabilityBiologyCDKN2AGeneticsDNA repair
-
The repetitive structure of genomic DNA holds many secrets to be discovered. A systematic study of repetitive DNA on a genomic or inter-genomic scale requires extensive algorithmic support. The REPuter program described herein was designed to serve as a fundam…
openalex
Stefan Kurtz
2001-11-15
置信度 0.72
BiologyComputational biologyScope (computer science)genomic DNARepeated sequence
-
Metagenomics (also referred to as environmental and community genomics) is the genomic analysis of microorganisms by direct extraction and cloning of DNA from an assemblage of microorganisms. The development of metagenomics stemmed from the ineluctable evidenc…
openalex
Jo Handelsman
2004-12-01
置信度 0.72
MetagenomicsBiologyEnvironmental DNAGenomeHorizontal gene transfer
-
One of the most pressing challenges in genomic medicine is to understand the role played by genetic variation in health and disease. Thanks to the exploration of genomic variants at large scale, hundreds of thousands of disease-associated loci have been uncove…
openalex
Janet Piñero, Juan Manuel Ramírez‐Anguita, Josep Saüch-Pitarch, Francesco Ronzano 等
2019-10-18
置信度 0.72
GenomicsInteroperabilityBiologySuiteStandardization
-
Comparative genomic hybridization produces a map of DNA sequence copy number as a function of chromosomal location throughout the entire genome. Differentially labeled test DNA and normal reference DNA are hybridized simultaneously to normal chromosome spreads…
openalex
Anne Kallioniemi, Olli Kallioniemi, Damir Sudar, Denis Rutovitz 等
1992-10-30
置信度 0.72
Comparative genomic hybridizationBiologyChromosomeMolecular biologyDNA
-
openalex
Alexis C. Komor, Y. Bill Kim, Michael S. Packer, John A. Zuris 等
2016-04-19
置信度 0.72
Genome editingIndelCRISPRCytidine deaminaseCas9
-
openalex
Shyue Ping Ong, William D. Richards, Anubhav Jain, Geoffroy Hautier 等
2012-12-08
置信度 0.72
Python (programming language)Computer scienceComputational scienceSoftwareApplication programming interface
-
openalex
Nicole M. Gaudelli, Alexis C. Komor, Holly A. Rees, Michael S. Packer 等
2017-10-24
置信度 0.72
DeaminationPoint mutationDNACRISPRCytosine
-
A large number of tiny noncoding RNAs have been cloned and named microRNAs (miRs). Recently, we have reported that miR-15a and miR-16a, located at 13q14, are frequently deleted and/or down-regulated in patients with B cell chronic lymphocytic leukemia, a disor…
openalex
George A. Calin, Cinzia Sevignani, Calin Dan Dumitru, Terry Hyslop 等
2004-02-18
置信度 0.72
Chromosomal fragile siteBiologymicroRNABreakpointGene
-
Reactive astrogliosis is characterized by a profound change in astrocyte phenotype in response to all CNS injuries and diseases. To better understand the reactive astrocyte state, we used Affymetrix GeneChip arrays to profile gene expression in populations of …
openalex
Jennifer Zamanian, Lijun Xu, Lynette C. Foo, Navid Nouri 等
2012-05-02
置信度 0.72
AstrogliosisAstrocyteGliosisTranscriptomeBiology
-
BACKGROUND: Diffuse low-grade and intermediate-grade gliomas (which together make up the lower-grade gliomas, World Health Organization grades II and III) have highly variable clinical behavior that is not adequately predicted on the basis of histologic class.…
openalex
The Cancer Genome Atlas Research Network
2015-06-11
置信度 0.72
ATRXGliomaMedicineDNA methylationExome
-
openalex
Vassily Trubetskoy, Antonio F. Pardiñas, Ting Qi, Georgia Panagiotaropoulou 等
2022-04-08
置信度 0.72
BiologySchizophrenia (object-oriented programming)GeneComputational biologyGenetics
-
openalex
Wolf Reik, Jörn Walter
2001-01-01
置信度 0.72
Genomic imprintingImprinting (psychology)EpigeneticsBiologyGenetics
-
openalex
Maxwell W. Libbrecht, William Stafford Noble
2015-05-07
置信度 0.72
Machine learningArtificial intelligenceComputer scienceGenomicsUnsupervised learning
-
openalex
David J. Lockhart, Elizabeth A. Winzeler
2000-06-01
置信度 0.72
GenomicsFunctional genomicsComputational biologyDNAGene
-
The PubMLST.org website hosts a collection of open-access, curated databases that integrate population sequence data with provenance and phenotype information for over 100 different microbial species and genera. Although the PubMLST website was conceived as pa…
openalex
Keith A. Jolley, James E. Bray, Martin Maiden
2018-09-24
置信度 0.72
Multilocus sequence typingGenomicsGenomePopulationBiology
-
openalex
Willy Hugo, Jesse M. Zaretsky, Lu Sun, Chunying Song 等
2016-03-01
置信度 0.72
BiologyMelanomaCancer researchTranscriptomeMAPK/ERK pathway
-
openalex
Oliver Fiehn, Joachim Kopka, Peter Dörmann, Thomas Altmann 等
2000-11-01
置信度 0.72
EcotypeMetabolomicsMetabolite profilingFunctional genomicsArabidopsis
-
openalex
Julie George, Jing Lim, Se Jin Jang, Yupeng Cun 等
2015-07-10
置信度 0.72
BiologyCancer researchSomatic cellGeneChromothripsis
-
openalex
Francis S. Collins, Eric D. Green, Alan E. Guttmacher, Mark S. Guyer
2003-04-14
置信度 0.72
BlueprintGenomicsComputational biologyData scienceBiology
-
openalex
Alice B. Popejoy, Stephanie M. Fullerton
2016-10-10
置信度 0.72
Diversity (politics)Precision medicineGenomicsComputational biologyBiology
-
openalex
Peter M. Visscher, William G. Hill, Naomi R. Wray
2008-03-04
置信度 0.72
HeritabilityBiologyMissing heritability problemGenomicsPopulation
-
openalex
En Li, Caroline Beard, Rudolf Jaenisch
1993-12-01
置信度 0.72
Genomic imprintingDNA methylationBiologyImprinting (psychology)Genetics
-
openalex
Benjamin B. Sun, Joseph Maranville, James E. Peters, David Stacey 等
2018-05-29
置信度 0.72
Mendelian randomizationProteomeBiologyExpression quantitative trait lociComputational biology
-
A cornerstone of modern biomedical research is the use of mouse models to explore basic pathophysiological mechanisms, evaluate new therapeutic approaches, and make go or no-go decisions to carry new drug candidates forward into clinical trials. Systematic stu…
openalex
Junhee Seok, H. Shaw Warren, Alex G. Cuenca, Michael Mindrinos 等
2013-02-11
置信度 0.72
Computational biologyHuman studiesTranslational medicineTranslational researchAnimal model
-
Functional annotation of novel sequence data is a primary requirement for the utilization of functional genomics approaches in plant research. In this paper, we describe the Blast2GO suite as a comprehensive bioinformatics tool for functional annotation of seq…
openalex
Ana Conesa, Stefan Götz
2008-04-30
置信度 0.72
AnnotationComputer scienceSuiteFunctional genomicsGenomics
-
There are currently few therapeutic options for patients with pancreatic cancer, and new insights into the pathogenesis of this lethal disease are urgently needed. Toward this end, we performed a comprehensive genetic analysis of 24 pancreatic cancers. We firs…
openalex
Siân Jones, Xiaosong Zhang, D. Williams Parsons, Jimmy Lin 等
2008-09-04
置信度 0.72
BiologyCarcinogenesisPancreatic cancerTranscriptomeGene
-
High-throughput sequencing based techniques, such as 16S rRNA gene profiling, have the potential to elucidate the complex inner workings of natural microbial communities - be they from the world's oceans or the human gut. A key step in exploring such data is t…
openalex
Jonathan Friedman, Eric J. Alm
2012-09-20
置信度 0.72
Spurious relationshipCompositional dataHuman Microbiome ProjectMicrobiomeProfiling (computer programming)