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Paper Details

Validity of Self-testing at Home With Rapid Severe Acute Respiratory Syndrome Coronavirus 2 Antibody Detection by Lateral Flow Immunoassay.
Clin Infect Dis
3
2023
Author NameAffiliation
Ara DarziImperial College Healthcare NHS Trust
Ara DarziInstitute of Global Health Innovation at Imperial College London
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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