grant
NHGRI/DIR Genomics Core
Organization NATIONAL HUMAN GENOME RESEARCH INSTITUTELocation UNITED STATES
NIHUS FederalResearch GrantFY202517p- syndromeAD/HDADHDAML - Acute Myeloid LeukemiaAcute Myeloblastic LeukemiaAcute Myelocytic LeukemiaAcute Myelogenous LeukemiaAllelic LossAttention deficit hyperactivity disorderBeadChipBioinformaticsBlood DiseasesBlood capillariesBrachydanio rerioBreast CancerCRISPRCRISPR approachCRISPR based approachCRISPR methodCRISPR methodologyCRISPR techniqueCRISPR technologyCRISPR toolsCRISPR-CAS-9CRISPR-based methodCRISPR-based techniqueCRISPR-based technologyCRISPR-based toolCRISPR/CAS approachCRISPR/Cas methodCRISPR/Cas systemCRISPR/Cas technologyCRISPR/Cas9CRISPR/Cas9 technologyCancersCardiac MalformationCas nuclease technologyCellular biologyClosure by LigationClustered Regularly Interspaced Short Palindromic RepeatsClustered Regularly Interspaced Short Palindromic Repeats approachClustered Regularly Interspaced Short Palindromic Repeats methodClustered Regularly Interspaced Short Palindromic Repeats methodologyClustered Regularly Interspaced Short Palindromic Repeats techniqueClustered Regularly Interspaced Short Palindromic Repeats technologyCole syndromeCole-Rauschkolb-Toomey syndromeCollectionColobomaColorectal CancerCommunicationCommunitiesComputer softwareCongenital PancytopeniaConsultationsCopy Number PolymorphismDNADanio rerioDataData AnalysesData AnalysisDeoxyribonucleic AcidDetectionDiabetes MellitusDiagnosisDiamond-Blackfan anemiaDyskeratosis CongenitaEngman syndromeEpilepsyEpileptic SeizuresEpilepticsEvaluationEventEye diseasesFanconi AnemiaFanconi PanmyelopathyFanconi dysplasiaFanconi's AnemiaFeverGaucher DiseaseGauchers DiseaseGeneticGenetics-MutagenesisGenomeGenomic SegmentGenomicsGenotypeHaplotypesHead and Neck CancerHead and Neck CarcinomaHeart MalformationHematologic DiseasesHematological DiseaseHematological DisorderHumanHuman Cell LineIBD analysisIBD inferenceInfectionInherited bone marrow failureInvestigatorsIslet CellKidney DiseasesLearningLeber congenital amaurosisLeber's amaurosisLeber's congenital amaurosisLigationLinkage DisequilibriumLong COVIDLong COVID-19Long coronavirus diseaseLong coronavirus disease 2019Loss of HeterozygosityMalignant Breast NeoplasmMalignant Head and Neck NeoplasmMalignant NeoplasmsMalignant TumorMethylationMiceMice MammalsModern ManMosaicismMurineMusMutagenesisMutagenesis Molecular BiologyNHGRINHLBINIAIDNIAMSNICHDNIMHNational Center for Human Genome ResearchNational Heart, Lung, and Blood InstituteNational Human Genome Research InstituteNational Institute of Allergy and Infectious DiseaseNational Institute of Arthritis, and Musculoskeletal, and Skin DiseasesNational Institute of Child Health and Human DevelopmentNational Institute of Mental HealthNational Institutes of HealthNephropathyOculocutaneous AlbinismParentsPatientsPredominantly Hyperactive-Impulsive Type Attention-Deficit DisorderPredominantly Hyperactive-Impulsive Type Hyperactivity DisorderPrimary Erythroid HypoplasiaProblem SolvingProcessPyrexiaRenal DiseaseResearchResearch PersonnelResearch ResourcesResearchersResourcesRunningSNP arraySNP chipSNP genotypingSamplingSeizure DisorderServicesSmith Magenis syndromeSoftwareSpeedSyndromeTechnologyUnited States National Institutes of HealthUpdateVariantVariationX-Linked Dyskeratosis CongenitaZFN technologyZFN-based systemZebra DanioZebra FishZebrafishZinsser syndromeZinsser-Engman-Cole syndromeabnormal heart developmentacute granulocytic leukemiaacute myeloid leukemiaamaurosis congenita of Leberbead chipblood disorderbone marrow failure syndromecapillarycell biologychromosome 17p deletion syndromechromosome 17p monosomychronic COVIDchronic COVID-19chronic novel coronavirus disease 2019congeniccongenital amaurosis of retinal origincongenital aplastic anemiacongenital cardiac abnormalitycongenital cardiac anomaliescongenital cardiac diseasecongenital cardiac disordercongenital cardiac malformationcongenital dyskeratosiscongenital heart abnormalitycongenital heart anomalycongenital heart diseasecongenital heart disordercongenital heart malformationconsultationcopy number variantcopy number variationdata accessdata interpretationdel(17p) syndromedeletion 17p syndromedeletion detectiondesigndesigningdiabetesepilepsiaepileptogenicexome sequencingexome-seqeye disorderfebrilefebrisgenome scalegenome segmentgenome-widegenomewidegenomic regionhead/neck cancerhuman DNAiPSiPSCiPSCsidentical by descentidentity by descentindelinduced pluripotent cellinduced pluripotent stem cellinducible pluripotent cellinducible pluripotent stem cellinherited disease of bone marrow failureinsertion/deletioninsertion/deletion mutationinterestkidney disorderlong haul COVIDlong haul COVID-19long haul coronavirus diseaselong haul coronavirus disease 2019long-hauler COVIDlong-hauler COVID-19long-hauler coronavirus disease 2019long-hauler syndromelong-term COVIDlong-term COVID-19long-term coronavirus diseaselong-term coronavirus disease 2019malignancymalignant breast tumormalignant head and neck tumormeetingmeetingsmonosomy 17pmosaicmosaic diseasesmosaic disordersmutation scanningmutation screeningneoplasm/cancerocular diseaseocular disorderophthalmopathyparentpersistent COVID-19population stratificationpost COVID syndromepost COVID-19 syndromepost acute COVID syndromepost acute COVID-19post acute COVID-19 syndromepost acute SARS-CoV-2post acute coronavirus disease 2019post acute coronavirus disease 2019 syndromepost acute coronavirus disease syndromepost acute severe acute respiratory syndrome coronavirus 2post coronavirus disease 2019 syndromepost coronavirus disease syndromepost-acute phases of COVID-19programsprolonged COVID-19 symptomsrenal disorderresearch studyservice utilizationsingle nucleotide polymorphism arraysingle nucleotide polymorphism chipsingle nucleotide polymorphism genotypingtoolzinc finger nuclease technology
Description preview
Genotyping services utilizing both Illumina and ABI technologies are used by investigators. This year, FY2025, in addition to two programs (NISC and UDP), four NHGRI investigators, representing four branches/offices, used the Core genotyping services. Outside of NHGRI, six investigators from other institutes (NCI, NIAID, NICHD, NHLBI, NIAMS, and…
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