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Hands-on experience in next-generation sequencing, e.g. Illumina, Oxford Nanopore or PacBio platforms with various sample types, including purified DNA, microbial, fresh and FFPE tissue material, blood, etc.
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Bachelor's degree and MT (ASCP) or CLS (NCA) certification; OR Bachelor's degree and CHT (ABHI) or CHS (ABHI) certification; OR Bachelor's degree and two (2) years of previous HLA experience or molecular genetics laboratory experience, preferably including DNA extractions, PCR amplification, probe hybridization/detection or DNA sequencing.
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Volta Labs is an MIT spin-off that has unlocked powerful new DNA sequencing capabilities by developing novel fluidic technology. Building off of this core technology, Volta has created a product that streamlines DNA sequencing sample prep.
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I am working directly with the founders of a rapidly growing privately owned consulting firm where making a difference is woven into their DNA, pushing at length their patient centric philosophy and head up by some of the industries most prestigious leaders.
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CATALOG, a Boston-based pioneering startup, is making significant strides in the field of data storage and computation by harnessing the power of DNA. DNA, known for its millennia-long stability, unrivaled information density, and cost-effective replicability, offers revolutionary potential for latency-tolerant high-density data storage and massively parallel computation.
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Provide assistance in the execution of experiments and analytical procedures including: molecular biology, DNA cloning, cell culture, protein production, ELISA, Biolayer interferometry and HPLC.
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CRISPR, RNA/DNA analyses (RNseq), immunohistochemistry, immunoprecipitation, immunoblotting, and general lab organization/safety. CRISPR, RNA/DNA analyses (RNseq), immunohistochemistry, immunoprecipitation, immunoblotting, and general lab organization/safety.
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Performs routine and non-routine laboratory tests which may include DNA sequencing, gene cloning, in situ hybridization, immunohistochemistry, northern blotting; synthesizes and interprets results.
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Experience in CLIA/CAP- processing patient samples- and manual molecular biology techniques, DNA/RNA extraction, qPCR, with pipetting at the very least. Current certification or eligible with ASCP (American Society of Clinical Pathologists) as an MLS - Medical Laboratory Scientist, MT - Medical Technologist, MLT-Medical Laboratory Technician, MB- Molecular Biology or specialist.
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ReciBioPharm, the biologics business unit of ReciPharm AB, is seeking a talented individual with background in Strain Engineering & Development to join our Plasmid Upstream Process Development team in Nucleic Acid PD Group in Watertwon, MA. The Sr. Scientist/Scientist will be accountable for developing bacterial cell line for plasmid DNA production and quality control of plasmid DNA product.
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The responsibilities will include RNA/DNA sample processing and data acquisition for microarray and sequencing analysis and routine maintenance of the Core equipment. Previous experience with microarray or next generation sequencing technology and Linux is not required, but helpful.
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Work within an interdisciplinary team of molecular biologists, computational biologists, software engineers, and scientific leaders focused on developing diagnostic products using massively parallel sequencing of tumor genomic DNA and RNA.
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Experience with clinical research, mouse handling, and standard molecular biology techniques (DNA/RNA extraction, cell cultures, PCR, western blot, immunostaining) Experience with clinical research, mouse handling, and standard molecular biology techniques (DNA/RNA extraction, cell cultures, PCR, western blot, immunostaining.
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2+ years of experience with standard mRNA workflow: e.g. plasmid/DNA linearization, purification, RNA synthesis by IVT, and purification. Perform experiments to produce DNA templates for in-vitro transcription.
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Proficiency in molecular biology techniques including DNA extraction and PCR. Proficiency in molecular biology techniques including DNA extraction and PCR. The Wheeler Laboratory in the Center for Genomic Medicine at Massachusetts General Hospital (MGH) study human diseases that are caused by expanded microsatellite repeats, with a principal focus on Huntington's disease (HD.
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