Yaniv Erlich

发表

Compressed sensing approach for high throughput carrier screen

Yaniv Erlich, Noam Shental, Amnon Amir, 2009, 2009 47th Annual Allerton Conference on Communication, Control, and Computing (Allerton).

Relative matching using low coverage sequencing

Yaniv Erlich, Regev Schweiger, Ella Petter, 2020 .

DNA Fountain enables a robust and efficient storage architecture

Yaniv Erlich, Dina Zielinski, Yaniv Erlich, 2016, Science.

Routes for breaching and protecting genetic privacy

Yaniv Erlich, Arvind Narayanan, Yaniv Erlich, 2013, Nature Reviews Genetics.

Capacity-approaching DNA storage

Yaniv Erlich, Dina Zielinski, Yaniv Erlich, 2016 .

A Vision for Ubiquitous Sequencing

Yaniv Erlich, 2015 .

Biological screens from linear codes: theory and tools

Atri Rudra, Hung Q. Ngo, Anna C. Gilbert, 2015, bioRxiv.

Profiling short tandem repeats from short reads.

Yaniv Erlich, Melissa Gymrek, M. Gymrek, 2013, Methods in molecular biology.

Re-identification of genomic data using long range familial searches

Yaniv Erlich, Tal Shor, Shai Carmi, 2018, bioRxiv.

Weighted pooling—practical and cost-effective techniques for pooled high-throughput sequencing

Yaniv Erlich, Saharon Rosset, David Golan, 2012, Bioinform..

Identity inference of genomic data using long-range familial searches

Yaniv Erlich, Tal Shor, Itsik Pe'er, 2018, Science.

FactorialHMM: Fast and exact inference in factorial hidden Markov models

Yaniv Erlich, Regev Schweiger, Shai Carmi, 2018 .

Review Routes for breaching and protecting genetic privacy

Yaniv Erlich, Arvind Narayanan, Yaniv Erlich, 2013 .

Identifying Personal Genomes by Surname Inference

Eran Halperin, Yaniv Erlich, Melissa Gymrek, 2013, Science.

lobSTR: A Short Tandem Repeat Profiler for Personal Genomes

Yaniv Erlich, Saharon Rosset, Melissa Gymrek, 2012, RECOMB.

A DNA-of-things storage architecture to create materials with embedded memory

Yaniv Erlich, Julian Koch, Robert N. Grass, 2019, Nature Biotechnology.

Compressed Genotyping

Michael Brand, Partha P. Mitra, Yaniv Erlich, 2009, IEEE Transactions on Information Theory.

Sci-LMM is an efficient strategy for inferring genetic variance components using population scale family trees

Dan Geiger, Yaniv Erlich, Tal Shor, 2018, bioRxiv.

DNA Fountain enables a robust and efficient storage architecture

Yaniv Erlich, Dina Zielinski, 2016 .

Author response: Using mobile sequencers in an academic classroom

Yaniv Erlich, Sophie Zaaijer, 2016 .

Base-Calling for Bioinformaticians

Yaniv Erlich, Mona Sheikh, Yaniv Erlich, 2012 .

Routes for breaching and protecting genetic privacy

Yaniv Erlich, Arvind Narayanan, 2013 .

DNA Compass: a secure, client-side site for navigating personal genetic information

Yaniv Erlich, Charles Curnin, Assaf Gordon, 2016, bioRxiv.

DNA Compass: a secure, client-side site for navigating personal genetic information

Yaniv Erlich, Charles Curnin, Assaf Gordon, 2016 .

FactorialHMM: Fast and exact inference in factorial hidden Markov models

Yaniv Erlich, Regev Schweiger, Shai Carmi, 2018, bioRxiv.

DNA.Land: A digital biobank using a massive crowdsourcing approach

Yaniv Erlich, Jie Yuan, Dina Zielinski, 2017 .

Integration of mobile sequencers in an academic classroom

Yaniv Erlich, Sophie Zaaijer, 2015 .

Redefining Genomic Privacy: Trust and Empowerment

Yaniv Erlich, Lincoln D. Stein, James B. Williams, 2014 .

Quantitative analysis of population-scale family trees using millions of relatives

Yaniv Erlich, Melissa Gymrek, Alkes L. Price, 2017, bioRxiv.

iPipet: sample handling using a tablet

Yaniv Erlich, Dina Zielinski, Assaf Gordon, 2014, Nature Methods.

Genome-wide profiling of heritable and de novo STR variations

Yaniv Erlich, Melissa Gymrek, Dina Zielinski, 2016, Nature Methods.

Quantitative analysis of population-scale family trees with millions of relatives

Dan Geiger, Yaniv Erlich, Melissa Gymrek, 2017, Science.

The landscape of human STR variation

Yaniv Erlich, Melissa Gymrek, Gareth Highnam, 2014, bioRxiv.

Genome-wide profiling of heritable and de novo STR variations

Yaniv Erlich, Melissa Gymrek, Dina Zielinski, 2016 .

Abundant contribution of short tandem repeats to gene expression variation in humans

Yaniv Erlich, Melissa Gymrek, Andrew J Sharp, 2015, Nature Genetics.

Estimating variance components in population scale family trees

Dan Geiger, Yaniv Erlich, Tal Shor, 2019, PLoS genetics.

Rapid re-identification of human samples using portable DNA sequencing

Yaniv Erlich, Assaf Gordon, Daniel Speyer, 2017, eLife.

Major flaws in “Identification of individuals by trait prediction using whole-genome sequencing data”

Yaniv Erlich, Yaniv Erlich, 2017, bioRxiv.

Punctuated bursts in human male demography inferred from 1,244 worldwide Y-chromosome sequences

Maria Cerezo, Paul Flicek, Yaniv Erlich, 2016, Nature Genetics.

Case–control association mapping by proxy using family history of disease

Yaniv Erlich, Joseph K. Pickrell, Yaniv Erlich, 2017, Nature Genetics.

Using mobile sequencers in an academic classroom

Yaniv Erlich, Sophie Zaaijer, Yaniv Erlich, 2016, eLife.

Democratizing DNA Fingerprinting

Yaniv Erlich, Assaf Gordon, Daniel Speyer, 2016, bioRxiv.

Exome sequencing and disease-network analysis of a single family implicate a mutation in KIF1A in hereditary spastic paraparesis.

Yaniv Erlich, Emily Hodges, G. Hannon, 2011, Genome research.

DNA.Land is a framework to collect genomes and phenomes in the era of abundant genetic information

Yaniv Erlich, Joseph K. Pickrell, Richard Aufrichtig, 2018, Nature Genetics.