Gianni Calogero Ferreri - Northford CT, US Jan F. Simons - San Francisco CA, US Michael Todd Ronan - New York NY, US Michael Egholm - Madison CT, US Brian C. Godwin - North Haven CT, US David Roderick Riches - Hamden CT, US Stephen Kyle Hutchison - Branford CT, US Michael S. Braverman - New Haven CT, US Melinda D. Palmer - Hamden CT, US Jeffrey Jeddeloh - Verona WI, US Jacob Kitzman - Seattle WA, US Thomas J. Albert - Verona WI, US
An embodiment of an adaptor element for efficient target processing is described that comprises a semi-complementary double stranded nucleic acid adaptor comprising a non-complementary region and a complementary region, where the non-complementary region comprises a first amplification primer site and a second amplification primer site and the complementary region comprises a sequencing primer site and one or more inosine species.
System And Method For Operation Of Isfet Arrays Using Ph Inert Reference Sensors
Gianni Calogero Ferreri - Northford CT, US Sagnik Basuray - Columbia MO, US Arthika Bappal - Bridgeport CT, US Suresh Gopalkrishna Shenoy - Branford CT, US Xavier Victor Gomes - Wallingford CT, US
International Classification:
C12Q 1/68 H01L 27/105
US Classification:
506 2, 506 16, 257253
Abstract:
An embodiment of a method for sequencing a species of nucleic acid template using pH inert reference sensors is described that comprises the steps of: introducing a nucleotide species to an array of wells where a plurality of the wells comprise a species of nucleic acid template and a plurality of the wells comprise a plurality of functional groups with a high pH buffering characteristic, and in at least a first well a polymerase species incorporates the nucleotide species into a plurality of strands complementary to the species of nucleic acid template disposed in the first well and results in a release of a plurality of hydrogen ions; detecting a signal in the first well that is responsive to the hydrogen ions and one or more noise sources; detecting a signal in a second well comprising the functional groups with the high pH buffering characteristic that is responsive to the one or more noise sources; and subtracting the second well signal from the first well signal to generate a corrected signal associated with the detected hydrogen ions.
Zhoutao Chen - Carlsbad CA, US Brian Christopher Godwin - North Haven CT, US Gianni Calogero Ferreri - Northford CT, US David Roderick Riches - Hamden CT, US
International Classification:
C12Q 1/68
US Classification:
435 6
Abstract:
An embodiment of a method for obtaining a DNA construct comprising two end regions of a target nucleic acid in an in vitro reaction is described that comprises the steps of: fragmenting a large nucleic acid molecule to produce a target nucleic acid molecule; ligating a recombination adaptor element to each end of the target nucleic acid molecule to produce an adapted target nucleic acid molecule; exposing the adapted target nucleic acid to a site specific recombinase to produce a circular nucleic acid product and a linear nucleic acid product from the adapted target nucleic acid, wherein the circular nucleic acid product comprises the target nucleic acid molecule; and fragmenting the circular nucleic acid product to produce a template nucleic acid molecule comprising a sequence region from each end of the target nucleic acid molecule.
Assessing Antigen Retrieval And Target Retrieval Progression With Vibrational Spectroscopy
- Tucson AZ, US David Chafin - Tucson AZ, US Bohuslav Dvorak - Tucson AZ, US Gianni Ferreri - Tucson AZ, US
International Classification:
G16B 40/20 G16B 25/10 G16H 10/40
Abstract:
The present disclosure relates to automated systems and methods for quantitatively determining an unmasking status of a biological specimen subjected to an unmasking process (e.g. an antigen retrieval process and/or a target retrieval process) using a trained unmasking status estimation engine. In some embodiments, the trained unmasking status estimation engine comprises a machine learning algorithm based on a projection onto latent structure regression model. In some embodiments, the trained unmasking status estimation engine includes a neural network.
- Branford CT, US Priya SHANBHAG - Rocky Hill CT, US Craig Elder MEALMAKER - Jersey City NJ, US Gianni Calogero FERRERI - Northford CT, US Melinda PALMER - Hamden CT, US Shally Hsueh-Wen WANG - Guilford CT, US
International Classification:
C12P 19/34 C12Q 1/68
Abstract:
An embodiment of a method for generating a population of amplified concatamer products is described that comprises amplifying a template nucleic acid molecule using a first nucleic acid primer immobilized on a bead substrate and a second nucleic acid primer in solution to generate a population of substantially identical copies of the template nucleic acid molecule immobilized on the bead substrate; and amplifying the population of substantially identical copies of the template nucleic acid molecule using a concatamer primer that comprises a first region complementary to an end region of the population of substantially identical copies of the template nucleic acid molecule and a second region to generate a population of immobilized concatamer products of the substantially identical copies of the template nucleic acid molecule.
- Branford CT, US Priya Shanbhag - Rocky Hill CT, US Craig Elder Mealmaker - Jersey City NJ, US Gianni Calogero Ferreri - Northford CT, US Melinda Palmer - Hamden CT, US Shally Hsueh-Wen Wang - Guilford CT, US
International Classification:
C12P 19/34
US Classification:
435 912
Abstract:
An embodiment of a method for generating a population of amplified concatamer products is described that comprises amplifying a template nucleic acid molecule using a first nucleic acid primer immobilized on a bead substrate and a second nucleic acid primer in solution to generate a population of substantially identical copies of the template nucleic acid molecule immobilized on the bead substrate; and amplifying the population of substantially identical copies of the template nucleic acid molecule using a concatamer primer that comprises a first region complementary to an end region of the population of substantially identical copies of the template nucleic acid molecule and a second region to generate a population of immobilized concatamer products of the substantially identical copies of the template nucleic acid molecule.
454 Life Sciences - Greater New York City Area since Mar 2013
Group Leader
454 Life Sciences - Greater New York City Area Mar 2011 - Feb 2013
Research Scientist III
454 Life Sciences - Greater New York City Area Mar 2009 - Feb 2011
Research Scientist II
454 Life Sciences - Greater New York City Area Apr 2008 - Feb 2009
Research Scientist I
University of Connecticut Sep 2001 - Dec 2007
Teaching Assistant
Education:
The University of Connecticut 2001 - 2007
The University of Connecticut 1997 - 2001
Skills:
Dna Sequencing Sequencing Genomics Molecular Biology Genetics Biotechnology Qpcr Life Sciences Rna Isolation Assay Development Pcr Dna Extraction Bioinformatics Fluorescence Tissue Culture Cell Biology Sample Preparation Primer Design Biochemistry Rt Pcr Dna Team Management Project Management Lifesciences R&D Agarose Gel Electrophoresis Cell Culture Sequence Analysis High Throughput Screening Fluorescence Microscopy Molecular Genetics Western Blotting Molecular Cloning Team Leadership Purification Elisa Cell Flow Cytometry In Situ Hybridization Genotyping Laboratory Protein Purification Protein Chemistry Microarray Analysis Proteomics Immunoassays
2013 to 2000 Group Leader454 Life Sciences, A Roche Company
2011 to 2013 Research Scientist III454 Life Sciences, A Roche Company
2009 to 2011 Research Scientist II454 Life Sciences, A Roche Company
2008 to 2009 Research Scientist I
Education:
University of Connecticut Storrs, CT Feb 2008 Ph.D. in Genetics and GenomicsUniversity of Connecticut Storrs, CT 2001 B.S. in Molecular and Cell Biology
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