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Paper Details

Machine learning identifies the independent role of dysplasia in the prediction of response to chemotherapy in AML.
Leukemia
3
2022
Author NameAffiliation
Matthieu DuchmannAssistance Publique-Hopitaux de Paris, Universite de Paris
Matthieu DuchmannUniversite de Paris, INSERM, CNRS
Claude GardinAssistance Publique-Hopitaux de Paris
Claude PreudhommeUniversite Lille, CNRS, INSERM
Herv?? DombretAssistance Publique-Hopitaux de Paris, Institut de Recherche Saint-Louis, Universite de Paris
Raphael ItzyksonUniversite de Paris, INSERM, CNRS
Raphael ItzyksonAssistance Publique-Hopitaux de Paris, Universite de Paris
Thomas CluzeauUniversite Cote d'Azur, CHU de Nice
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Datasets

Allele Frequency AggregatorThe NCBI Allele Frequency Aggregator (ALFA) seeks to make allele frequency datasets from dbGaP studies the largest and most complete aggregated variant datasets available as open-access. Over two million individuals, up to billions of variations, thousands of phenotypes, and molecular test datasets make up the database dbGaP. Huge opportunities exist to investigate and research genetic differences within human populations and to find genetic factors that affect health and diseases in order to enhance diagnosis, treatment, and prevention.Link
Allele Frequency AggregatorThe NCBI Allele Frequency Aggregator (ALFA) seeks to make allele frequency datasets from dbGaP studies the largest and most complete aggregated variant datasets available as open-access. Over two million individuals, up to billions of variations, thousands of phenotypes, and molecular test datasets make up the database dbGaP. Huge opportunities exist to investigate and research genetic differences within human populations and to find genetic factors that affect health and diseases in order to enhance diagnosis, treatment, and prevention.Link
Allele Frequency AggregatorThe NCBI Allele Frequency Aggregator (ALFA) seeks to make allele frequency datasets from dbGaP studies the largest and most complete aggregated variant datasets available as open-access. Over two million individuals, up to billions of variations, thousands of phenotypes, and molecular test datasets make up the database dbGaP. Huge opportunities exist to investigate and research genetic differences within human populations and to find genetic factors that affect health and diseases in order to enhance diagnosis, treatment, and prevention.Link
Allele Frequency AggregatorThe NCBI Allele Frequency Aggregator (ALFA) seeks to make allele frequency datasets from dbGaP studies the largest and most complete aggregated variant datasets available as open-access. Over two million individuals, up to billions of variations, thousands of phenotypes, and molecular test datasets make up the database dbGaP. Huge opportunities exist to investigate and research genetic differences within human populations and to find genetic factors that affect health and diseases in order to enhance diagnosis, treatment, and prevention.Link
Allele Frequency AggregatorThe NCBI Allele Frequency Aggregator (ALFA) seeks to make allele frequency datasets from dbGaP studies the largest and most complete aggregated variant datasets available as open-access. Over two million individuals, up to billions of variations, thousands of phenotypes, and molecular test datasets make up the database dbGaP. Huge opportunities exist to investigate and research genetic differences within human populations and to find genetic factors that affect health and diseases in order to enhance diagnosis, treatment, and prevention.Link
Allele Frequency AggregatorThe NCBI Allele Frequency Aggregator (ALFA) seeks to make allele frequency datasets from dbGaP studies the largest and most complete aggregated variant datasets available as open-access. Over two million individuals, up to billions of variations, thousands of phenotypes, and molecular test datasets make up the database dbGaP. Huge opportunities exist to investigate and research genetic differences within human populations and to find genetic factors that affect health and diseases in order to enhance diagnosis, treatment, and prevention.Link
Allele Frequency AggregatorThe NCBI Allele Frequency Aggregator (ALFA) seeks to make allele frequency datasets from dbGaP studies the largest and most complete aggregated variant datasets available as open-access. Over two million individuals, up to billions of variations, thousands of phenotypes, and molecular test datasets make up the database dbGaP. Huge opportunities exist to investigate and research genetic differences within human populations and to find genetic factors that affect health and diseases in order to enhance diagnosis, treatment, and prevention.Link
Allele Frequency AggregatorThe NCBI Allele Frequency Aggregator (ALFA) seeks to make allele frequency datasets from dbGaP studies the largest and most complete aggregated variant datasets available as open-access. Over two million individuals, up to billions of variations, thousands of phenotypes, and molecular test datasets make up the database dbGaP. Huge opportunities exist to investigate and research genetic differences within human populations and to find genetic factors that affect health and diseases in order to enhance diagnosis, treatment, and prevention.Link
Allele Frequency AggregatorThe NCBI Allele Frequency Aggregator (ALFA) seeks to make allele frequency datasets from dbGaP studies the largest and most complete aggregated variant datasets available as open-access. Over two million individuals, up to billions of variations, thousands of phenotypes, and molecular test datasets make up the database dbGaP. Huge opportunities exist to investigate and research genetic differences within human populations and to find genetic factors that affect health and diseases in order to enhance diagnosis, treatment, and prevention.Link
Allele Frequency AggregatorThe NCBI Allele Frequency Aggregator (ALFA) seeks to make allele frequency datasets from dbGaP studies the largest and most complete aggregated variant datasets available as open-access. Over two million individuals, up to billions of variations, thousands of phenotypes, and molecular test datasets make up the database dbGaP. Huge opportunities exist to investigate and research genetic differences within human populations and to find genetic factors that affect health and diseases in order to enhance diagnosis, treatment, and prevention.Link
Allele Frequency AggregatorThe NCBI Allele Frequency Aggregator (ALFA) seeks to make allele frequency datasets from dbGaP studies the largest and most complete aggregated variant datasets available as open-access. Over two million individuals, up to billions of variations, thousands of phenotypes, and molecular test datasets make up the database dbGaP. Huge opportunities exist to investigate and research genetic differences within human populations and to find genetic factors that affect health and diseases in order to enhance diagnosis, treatment, and prevention.Link