Skip to Main Content

Paper Details

LSC17 score complements genetics and measurable residual disease in acute myeloid leukemia: an ALFA study.
Blood Adv
3
2023
Author NameAffiliation
Herv?? DombretSt-Louis University Hospital
Claude PreudhommeCNRS, INSERM, University of Lille
Claude PreudhommeCentre Hospitalier Universitaire (CHU) Lille
Raphael ItzyksonSt-Louis University Hospital
Raphael ItzyksonINSERM, CNRS, Universite Paris Cite
  • 1 - 5

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