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Single Cell calculator
Single-Cell Sequencing Calculator
Whole Genome calculator - not ppmSeq
Whole Genome Sequencing Calculator
Bulk RNA calculator
Bulk RNA Sequencing Calculator
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Visium HD calculator
Visium HD Sequencing Wafer Use Calculator
Minimum Recommendations: 3' Universal : 550M reads per sample Probe :250M reads per sample
Technical Support Request
Have a question about your Ultima Genomics Sequencing experiment and Looking for expert support? Get connected with a technical support specialist who can help you find the right answer to your sequencing question. Whether you have questions about experimenal planning, library preparation, Loading/pooling samples, Bioinformatics or IT, our team is here to assist you.
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We’re proud to have been chosen by Ultima Genomics, from a competitive pool of applicants, to receive complimentary sequencing through the "Counts on Us" initiative. We’re excited to see how Ultima can enhance our capabilities as an Olink Certified Service Provider to deliver high-quality, data-rich services to our clients more efficiently. We’re thrilled to contribute to this innovative program and look forward to continued partnership on future screening projects.
Mariam IskilovaLTRI at Mout Sinai Hospital
At the Leshchiner Lab, we focus on cancer computational biology and cancer genetics. We apply new genomic technologies, computational analysis and AI methods on data from patients' tumors to understand the biology behind tumor development, treatment evasions, and progress to metastisis. Because we work with cfDNA requiring deep sequencing, we are eager to explore a more cost-effective, high-quality NGS technology to support our research needs. We are excited our project was chosen for the “Count on Us” initiative and hope to continue more projects using the Ultima platform in the future.
Ignaty Leshchiner, PhDBoston University School of Medicine
I’m incredibly excited and grateful for the support of the “Count on Us” initiative. Thrilled to be involved in the first transcriptomic dataset capturing how intestinal fibrosis starts and progresses in Crohn’s disease-like in vivo models, which has the potential to bring us closer to breakthroughs for IBD patients. This incredible support is a game-changer for my career and a unique chance to unlock insights for the entire IBD research community by tackling a process impossible to study directly in patients.
Stefania De Santis, PhDCase Western Reserve University
In the Humphrey Lab, we're pushing the limits of single-cell transcriptomics to study neurodegenerative disease. Through the "Count on Us" initiative, Ultima is empowering us to sequence patient brain samples far more deeply than before to uncover pathological changes in mRNA splicing in frontotemporal dementia. We're using Ultima to sequence over a million single cells sorted from patient brains at unprecedented sequencing coverage and depth. Our goal is to use the dataset to identify splicing changes in specific neuronal populations, identify new biomarkers of disease, and uncover the links between protein pathology and neuronal health.
Jack Humphrey, PhDMt. Sinai School of Medicine
We were thrilled when we got the news our proposal to resequence the Sorghum Diversity panel had been selected for the "Count on Us" initiative. Having high density genetic marker information for this population will help many research groups around the world accelerate their work to understand and improve this drought tolerant crop that plays an essential role in ensuring the food security of hundreds of millions of people.
James C. Schnable, PhDUniversity of Nebraska - Lincoln
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We’re proud to have been chosen by Ultima Genomics, from a competitive pool of applicants, to receive complimentary sequencing through the "Counts on Us" initiative.
Mariam IskilovaLTRI at Mout Sinai Hospital
At the Leshchiner Lab, we focus on cancer computational biology and cancer genetics. We apply new genomic technologies, computational analysis and AI methods on data from patients' tumors to understand the biology behind tumor development, treatment evasions, and progress to metastisis. Because we work with cfDNA requiring deep sequencing, we are eager to explore a more cost-effective, high-quality NGS technology to support our research needs.
Ignaty Leshchiner, PhDBoston University School of Medicine
I’m incredibly excited and grateful for the support of the “Count on Us” initiative. Thrilled to be involved in the first transcriptomic dataset capturing how intestinal fibrosis starts and progresses in Crohn’s disease-like in vivo models, which has the potential to bring us closer to breakthroughs for IBD patients.
Stefania De Santis, PhDCase Western Reserve University
In the Humphrey Lab, we're pushing the limits of single-cell transcriptomics to study neurodegenerative disease. Through the "Count on Us" initiative, Ultima is empowering us to sequence patient brain samples far more deeply than before to uncover pathological changes in mRNA splicing in frontotemporal dementia.
Jack Humphrey, PhDMt. Sinai School of Medicine
We were thrilled when we got the news our proposal to resequence the Sorghum Diversity panel had been selected for the "Count on Us" initiative.
James C. Schnable, PhDUniversity of Nebraska - Lincoln
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Whole Genome Wafer Capacity Calculator
calculate the number of wafers needed for your whole genome sequencing experiment based on the required depth of sequencing and input DNA type/treatment
Whole Genome Sequencing Resources:
link to protocol for Germline
link to protocol for Somatic
Link to EMSeq