Inventor · disambiguated record
Michael A. Eberle
Also filed as: EBERLE MICHAEL · EBERLE MICHAEL A
2 granted patents·14 pending applications·2 citations·filing 2013–2025
39Inventor score
Top patents by PatentIndex Score
16 records- 0176US10699801B2Detecting repeat expansions with short read sequencing dataILLUMINA CAMBRIDGE LTD·Filed 2015·Granted Jun 30, 2020·2 cites·24 claims
- 0267US2025356946A1Methods and systems for diagnosing from whole genome sequencing dataILLUMINA INC·Filed 2025·Application pending·0 cites
- 0365US2024112753A1Target-variant-reference panel for imputing target variantsILLUMINA INC·Filed 2023·Application pending·0 cites
- 0463US2023386608A1Targeted calling of overlapping copy number variantsILLUMINA INC·Filed 2023·Application pending·0 cites
- 0562US2025259701A1Methods and systems for identifying gene variantsILLUMINA INC·Filed 2023·Application pending·0 cites
- 0662US2023326549A1Copy number variant calling for lpa kiv-2 repeatILLUMINA INC·Filed 2023·Application pending·0 cites
- 0761US2021166781A1Methods and systems for diagnosing from whole genome sequencing dataILLUMINA INC·Filed 2020·Application pending·0 cites
- 0860US2020335178A1Detecting repeat expansions with short read sequencing dataILLUMINA CAMBRIDGE LTD·Filed 2020·Application pending·0 cites
- 0957US2023313271A1Machine-learning models for detecting and adjusting values for nucleotide methylation levelsILLUMINA INC·Filed 2023·Application pending·0 cites
- 1056US2023207049A1Determining pathogenic rfc1 expansions from sequencing dataILLUMINA INC·Filed 2022·Application pending·0 cites
- 1155US2023053523A1Methods and systems for identifying recombinant variantsILLUMINA INC·Filed 2022·Application pending·0 cites
- 1254US2023095961A1Graph reference genome and base-calling approach using imputed haplotypesILLUMINA INC·Filed 2022·Application pending·0 cites
- 1353US2023019053A1Genotyping variable number tandem repeatsILLUMINA INC·Filed 2022·Application pending·0 cites
- 1448US2022254442A1Methods and systems for visualizing short reads in repetitive regions of the genomeILLUMINA INC·Filed 2021·Application pending·0 cites
- 1547US12374422B2Sequence-graph based tool for determining variation in short tandem repeat regionsILLUMINA INC·Filed 2020·Granted Jul 29, 2025·0 cites·23 claims
- 1646US2013261984A1Methods and systems for determining fetal chromosomal abnormalitiesEBERLE MICHAEL A·Filed 2013·Application pending·0 cites
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Identity basis: PatentsView inventor disambiguation (2025Q4-odp release). How scoring works →