Human Genome Sequencing Using Unchained Base Reads on Self-Assembling DNA Nanoarrays

Initial sequencing and analysis of the human genome

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The sequence of the human genome

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Genome sequencing in microfabricated high-density picolitre reactors

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Next-generation DNA sequencing

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A second generation human haplotype map of over 3.1 million SNPs

The International HapMap Consortium (2007) · Nature · doi:10.1038/nature06258 · Cited by 4,438

Accurate whole human genome sequencing using reversible terminator chemistry

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The complete genome of an individual by massively parallel DNA sequencing

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The Diploid Genome Sequence of an Individual Human

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Mutation detection and single-molecule counting using isothermal rolling-circle amplification

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DNA sequencing of a cytogenetically normal acute myeloid leukaemia genome

Ley, T. J., Mardis, E. R., Ding, L., Fulton, B., McLellan, M. D., Chen, K., Dooling, D. J., Dunford-Shore, B. H., McGrath, S. D., Hickenbotham, M. T., et al. (2008) · Nature · doi:10.1038/nature07485 · Cited by 1,434

Khoe-San Genomes Reveal Unique Variation and Confirm the Deepest Population Divergence in Homo sapiens

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Nanochannel confinement: DNA stretch approaching full contour length

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VAAST 2.0: Improved Variant Classification and Disease‐Gene Identification Using a Conservation‐Controlled Amino Acid Substitution Matrix

Hu, H., Huff, C. D., Moore, B., Flygare, S. D., Reese, M. G., & Yandell, M. D. (2013) · Genetic Epidemiology · doi:10.1002/gepi.21743 · Cited by 143

Identical but not the same: The value of discordant monozygotic twins in genetic research

Zwijnenburg, P. J. G., Meijers-Heijboer, H. E. J., & Boomsma, D. I. (2010) · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · doi:10.1002/ajmg.b.31091 · Cited by 140

Next-Generation Sequencing Techniques for Eukaryotic Microorganisms: Sequencing-Based Solutions to Biological Problems

Nowrousian, M. (2010) · Eukaryotic Cell · doi:10.1128/ec.00123-10 · Cited by 145

A Selective Sweep on a Deleterious Mutation in CPT1A in Arctic Populations

Clemente, F., Cardona, A., Inchley, C. E., Peter, B. M., Jacobs, G. S., Pagani, L., Lawson, D. J., Antão, T., Vicente, M., Mitt, M., et al. (2014) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2014.09.016 · Cited by 147

Next-generation sequencing technologies and applications for human genetic history and forensics

Berglund, E., Kiialainen, A., & Syvänen, A. (2011) · Investigative Genetics · doi:10.1186/2041-2223-2-23 · Cited by 146

Phylogeny Estimation by Integration over Isolation with Migration Models

Hey, J., Chung, Y., Sethuraman, A., Lachance, J., Tishkoff, S. A., Sousa, V. C., & Wang, Y. (2018) · Molecular Biology and Evolution · doi:10.1093/molbev/msy162 · Cited by 140

Estimating genotype error rates from high-coverage next-generation sequence dataPreprint

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Extensive genomic and transcriptional diversity identified through massively parallel DNA and RNA sequencing of eighteen Korean individuals

Ju, Y. S., Kim, J., Kim, S., Hong, D., Park, H., Shin, J.-Y., Lee, S., Lee, W., Kim, S.-J., Yu, S.-B., et al. (2011) · Nature Genetics · doi:10.1038/ng.872 · Cited by 140

Personal genome sequencing: current approaches and challengesPreprint

Snyder, M. P., Du, J., & Gerstein, M. (2010) · Genes & Development · doi:10.1101/gad.1864110 · Cited by 145

MBASED: allele-specific expression detection in cancer tissues and cell lines

Mayba, O., Gilbert, H., Liu, J., Haverty, P. M., Jhunjhunwala, S., Jiang, Z., Watanabe, C. K., & Zhang, Z. (2014) · Genome biology · doi:10.1186/s13059-014-0405-3 · Cited by 138

Global population-specific variation in miRNA associated with cancer risk and clinical biomarkers

Rawlings-Goss, R., Campbell, M. C., & Tishkoff, S. A. (2014) · BMC Medical Genomics · doi:10.1186/1755-8794-7-53 · Cited by 139

Novel genetic and epigenetic factors of importance for inter-individual differences in drug disposition, response and toxicity

Lauschke, V. M., Zhou, Y., & Ingelman‐Sundberg, M. (2019) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2019.01.002 · Cited by 135

Controlled Translocation of Individual DNA Molecules through Protein Nanopores with Engineered Molecular Brakes

Rincón-Restrepo, M., Mikhailova, E., Bayley, H., & Maglia, G. (2011) · Nano Letters · doi:10.1021/nl1038874 · Cited by 136

Genome-wide inference of natural selection on human transcription factor binding sites

Arbiza, L., Gronau, I., Aksoy, B. A., Hubisz, M. J., Gulko, B., Keinan, A., & Siepel, A. C. (2013) · Nature Genetics · doi:10.1038/ng.2658 · Cited by 131

Overview of DNA Sequencing Strategies

Shendure, J., Porreca, G. J., Church, G. M., Gardner, A. F., Hendrickson, C. L., Kieleczawa, J., & Slatko, B. E. (2011) · Current Protocols in Molecular Biology · doi:10.1002/0471142727.mb0701s96 · Cited by 136

Targeted and genome-wide sequencing reveal single nucleotide variations impacting specificity of Cas9 in human stem cells

Yang, L., Grishin, D., Wang, G., Aach, J., Zhang, C., Chari, R., Homsy, J. G., Cai, X., Zhao, Y., Fan, J., et al. (2014) · Nature Communications · doi:10.1038/ncomms6507 · Cited by 133

Exploitation of Gene Expression and Cancer Biomarkers in Paving the Path to Era of Personalized Medicine

Kamel, H. F. M., & Al-Amodi, H. S. A. B. (2017) · Genomics Proteomics & Bioinformatics · doi:10.1016/j.gpb.2016.11.005 · Cited by 137

Next-generation sequencing technologies: breaking the sound barrier of human genetics

Bahassi, E. M., & Stambrook, P. J. (2014) · Mutagenesis · doi:10.1093/mutage/geu031 · Cited by 138

Targeted DNA sequencing and in situ mutation analysis using mobile phone microscopy

Kühnemund, M., Wei, Q., Darai, E., Wang, Y., Hernández-Neuta, I., Yang, Z., Tseng, D. K., Ahlford, A., Mathot, L., Sjöblom, T., et al. (2017) · Nature Communications · doi:10.1038/ncomms13913 · Cited by 131

Application of metagenomic next-generation sequencing in the diagnosis of infectious diseases

Zhao, Y., Zhang, W., & Zhang, X. (2024) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2024.1458316 · Cited by 147

Comparative performance of the BGISEQ-500 and Illumina HiSeq4000 sequencing platforms for transcriptome analysis in plants

Zhu, F., Chen, M., Ye, N., Qiao, W.-M., Gao, B., Law, W.-K., Tian, Y., Zhang, D., Zhang, D., Liu, T.-Y., et al. (2018) · Plant Methods · doi:10.1186/s13007-018-0337-0 · Cited by 138

Addressing the concerns of the lacks family

Humbert, M., Ayday, E., Hubaux, J., & Telenti, A. (2013) · ACM SIGSAC Conference on Computer and Communications Security (CCS) · doi:10.1145/2508859.2516707 · Cited by 132

Genomic dark matter: the reliability of short read mapping illustrated by the genome mappability score

Lee, H., & Schatz, M. C. (2012) · Bioinformatics · doi:10.1093/bioinformatics/bts330 · Cited by 129

Detecting recent selective sweeps while controlling for mutation rate and background selection

Huber, C. D., DeGiorgio, M., Hellmann, I., & Nielsen, R. (2015) · Molecular Ecology · doi:10.1111/mec.13351 · Cited by 126

Type 2 Diabetes Risk Alleles Demonstrate Extreme Directional Differentiation among Human Populations, Compared to Other Diseases

Chen, R., Corona, E., Sikora, M., Dudley, J. T., Morgan, A. A., Moreno‐Estrada, A., Nilsen, G. B., Ruau, D., Lincoln, S. E., Bustamante, C. D., et al. (2012) · PLoS Genetics · doi:10.1371/journal.pgen.1002621 · Cited by 129

Hypertrophic cardiomyopathy: from genetics to treatment

Marian, A. J. (2010) · European Journal of Clinical Investigation · doi:10.1111/j.1365-2362.2010.02268.x · Cited by 126

Layer-by-Layer Assembled Antisense DNA Microsponge Particles for Efficient Delivery of Cancer Therapeutics

Roh, Y. H., Lee, J. B., Shopsowitz, K. E., Dreaden, E. C., Morton, S. W., Poon, Z., Hong, J., Yamin, I., Bonner, D. K., & Hammond, P. T. (2014) · ACS Nano · doi:10.1021/nn502596b · Cited by 125

The contributions of rare inherited and polygenic risk to ASD in multiplex families

Cirnigliaro, M., Chang, T. S., Arteaga, S. A., Pérez‐Cano, L., Ruzzo, E. K., Gordon, A., Bicks, L. K., Jung, J.-Y., Lowe, J. K., Wall, D. P., et al. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2215632120 · Cited by 124

Recurrent chromosomal gains and heterogeneous driver mutations characterise papillary renal cancer evolution

Kovac, M. B., Navas, C., Horswell, S. D., Salm, M., Bardella, C., Rowan, A., Stares, M., Castro-Giner, F., Fisher, R. A., de Bruin, E. C., et al. (2015) · Nature Communications · doi:10.1038/ncomms7336 · Cited by 123

Diagnostic value of exome and whole genome sequencing in craniosynostosis

Miller, K. A., Twigg, S. R. F., McGowan, S. J., Phipps, J. M., Fenwick, A. L., Johnson, D., Wall, S. A., Noons, P., Rees, K. E. M., Tidey, E. A., et al. (2016) · Journal of Medical Genetics · doi:10.1136/jmedgenet-2016-104215 · Cited by 121

Merkel Cell Polyomavirus Exhibits Dominant Control of the Tumor Genome and Transcriptome in Virus-Associated Merkel Cell Carcinoma

Starrett, G. J., Marcelus, C., Cantalupo, P. G., Katz, J. P., Cheng, J., Akagi, K., Thakuria, M., Rabinowits, G., Wang, L. C., Symer, D. E., et al. (2017) · mBio · doi:10.1128/mbio.02079-16 · Cited by 126

Long read nanopore sequencing for detection of HLA and CYP2D6 variants and haplotypes

Ammar, R., Paton, T., Torti, D., Shlien, A., & Bader, G. D. (2015) · F1000Research · doi:10.12688/f1000research.6037.1 · Cited by 119

Evolutionary history of Tibetans inferred from whole-genome sequencing

Hu, H., Petousi, N., Glusman, G., Yu, Y., Bohlender, R. J., Tashi, T., Downie, J. M., Roach, J. C., Cole, A. M., Lorenzo, F., et al. (2017) · PLoS Genetics · doi:10.1371/journal.pgen.1006675 · Cited by 128

Inter-laboratory evaluation of SNP-based forensic identification by massively parallel sequencing using the Ion PGM™

Eduardoff, M., Santos, C., de la Puente, M., Gross, T. E., Fondevila, M., Strobl, C., Sobrino, B., Ballard, D., Schneider, P. M., Carracedo, Á., et al. (2015) · Forensic Science International Genetics · doi:10.1016/j.fsigen.2015.04.007 · Cited by 119

Defects of mutant DNMT1 are linked to a spectrum of neurological disorders

Baets, J., Duan, X., Wu, Y., Smith, G. A., Seeley, W. W., Mademan, I., McGrath, N. M., Beadell, N. C., Khoury, J. A., Botuyan, M. V., et al. (2015) · Brain · doi:10.1093/brain/awv010 · Cited by 127

Recessive mutations in SLC13A5 result in a loss of citrate transport and cause neonatal epilepsy, developmental delay and teeth hypoplasia

Hardies, K., de Kovel, C. G. F., Weckhuysen, S., Asselbergh, B., Geuens, T., Deconinck, T., Azmi, A., May, P., Brilstra, E. H., Becker, F., et al. (2015) · Brain · doi:10.1093/brain/awv263 · Cited by 118

Urinary bacteria in adult women with urgency urinary incontinence

Brubaker, L. T., Nager, C. W., Richter, H. E., Visco, A. G., Nygaard, I., Barber, M. D., Schaffer, J. I., Meikle, S., Wallace, D., Shibata, N., et al. (2014) · International Urogynecology Journal · doi:10.1007/s00192-013-2325-2 · Cited by 116

Natural Selection Reduced Diversity on Human Y Chromosomes

Sayres, M. A. W., Lohmueller, K. E., & Nielsen, R. (2014) · PLoS Genetics · doi:10.1371/journal.pgen.1004064 · Cited by 120

Molecular and Clinical Evidence for anARMC5Tumor Syndrome: Concurrent Inactivating Germline and Somatic Mutations Are Associated With Both Primary Macronodular Adrenal Hyperplasia and Meningioma

Elbelt, U., Trovato, A., Kloth, M. T., Gentz, E., Finke, R., Spranger, J., Galas, D. J., Weber, S. N., Wolf, C., König, K., et al. (2014) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2014-2648 · Cited by 120

Microfluidic chemical analysis systems.

Livak-Dahl, E., Sinn, I., & Burns, M. (2011) · Annual Review of Chemical and Biomolecular Engineering · doi:10.1146/annurev-chembioeng-061010-114215 · Cited by 105

Human genome diversity: frequently asked questions

Barbujani, G., & Colonna, V. (2010) · Trends in Genetics · doi:10.1016/j.tig.2010.04.002 · Cited by 117

Deficient H2A.Z deposition is associated with genesis of uterine leiomyoma

Berta, D. G., Kuisma, H., Välimäki, N., Räisänen, M., Jäntti, M., Pasanen, A. M., Karhu, A., Tolvanen, J., Taira, A., Cajuso, T., et al. (2021) · Nature · doi:10.1038/s41586-021-03747-1 · Cited by 111

Human genetics and genomics a decade after the release of the draft sequence of the human genome

Naidoo, N., Yudi Pawitan, Y., Soong, R., Cooper, D. N., & Ku, C. (2011) · Human Genomics · doi:10.1186/1479-7364-5-6-577 · Cited by 117

Taxonomizing, sizing, and overcoming the incidentalome

Kohane, I. S., Hsing, M., & Kong, S. W. (2012) · Genetics in Medicine · doi:10.1038/gim.2011.68 · Cited by 114

A standard variation file format for human genome sequences

Reese, M. G., Moore, B., Batchelor, C. R., Salas, F., Cunningham, F. M., Marth, G., Stein, L. D., Flicek, P., Yandell, M. D., & Eilbeck, K. L. (2010) · Genome biology · doi:10.1186/gb-2010-11-8-r88 · Cited by 112

Significance of TP53 Mutation in Wilms Tumors with Diffuse Anaplasia: A Report from the Children's Oncology Group

Ooms, A. H. A. G., Gadd, S., Gerhard, D. S., Smith, M. A., Auvil, J. M. G., Meerzaman, D. M., Chen, Q.-R., Hsu, C. H., Yan, C., Nguyen, C. D., et al. (2016) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-16-0985 · Cited by 110

Germline Variation in Cancer-Susceptibility Genes in a Healthy, Ancestrally Diverse Cohort: Implications for Individual Genome Sequencing

Bodian, D. L., McCutcheon, J. N., Kothiyal, P., Huddleston, K., Iyer, R. K., Vockley, J. G., & Niederhuber, J. E. (2014) · PLoS ONE · doi:10.1371/journal.pone.0094554 · Cited by 110

Patents in Genomics and Human Genetics

Cook-Deegan, R. M., & Heaney, C. D. (2010) · Annual Review of Genomics and Human Genetics · doi:10.1146/annurev-genom-082509-141811 · Cited by 108

IL-7 Receptor Mutations and Steroid Resistance in Pediatric T cell Acute Lymphoblastic Leukemia: A Genome Sequencing Study

Li, Y., Buijs-Gladdines, J. G. C. A. M., Canté-Barrett, K., Stubbs, A., Vroegindeweij, E. M., Smits, W. K., van Marion, R., Dinjens, W. N. M., Horstmann, M. A., Kuiper, R. P., et al. (2016) · PLoS Medicine · doi:10.1371/journal.pmed.1002200 · Cited by 111

Next generation sequencing: implications in personalized medicine and pharmacogenomics

Rabbani, B., Nakaoka, H., Akhondzadeh, S., Tekin, M., & Mahdieh, N. (2016) · Molecular BioSystems · doi:10.1039/c6mb00115g · Cited by 109

Model-based analyses of whole-genome data reveal a complex evolutionary history involving archaic introgression in Central African Pygmies

Hsieh, P., Woerner, A. E., Wall, J. D., Lachance, J., Tishkoff, S. A., Gutenkunst, R. N., & Hammer, M. F. (2016) · Genome Research · doi:10.1101/gr.196634.115 · Cited by 105

Genome Sequencing Explores Complexity of Chromosomal Abnormalities in Recurrent Miscarriage

Dong, Z., Yan, J., Xu, F., Yuan, J., Jiang, H., Wang, H., Chen, H., Zhang, L., Ye, L., Xu, J., et al. (2019) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2019.10.003 · Cited by 104

Whole exome sequencing reveals mutations inNARS2andPARS2, encoding the mitochondrial asparaginyl-tRNA synthetase and prolyl-tRNA synthetase, in patients with Alpers syndrome

Sofou, K., Kollberg, G., Holmström, M., López, M. D., Darín, N., Gustafsson, C. M., Holme, E., Oldfors, A., Tulinius, M., & Asin-Cayuela, J. (2014) · Molecular Genetics & Genomic Medicine · doi:10.1002/mgg3.115 · Cited by 104

DNA sequencing – spanning the generations

McGinn, S., & Gut, I. G. (2012) · New Biotechnology · doi:10.1016/j.nbt.2012.11.012 · Cited by 118

Modeling kinetic rate variation in third generation DNA sequencing data to detect putative modifications to DNA basesPreprint

Schadt, E. E., Banerjee, O., Fang, G., Feng, Z., Wong, W. H., Zhang, X., Kislyuk, A. O., Clark, T. A., Luong, K., Keren‐Paz, A., et al. (2012) · Genome Research · doi:10.1101/gr.136739.111 · Cited by 105

Ancient Structure in Africa Unlikely to Explain Neanderthal and Non-African Genetic Similarity

Yang, M. A., Malaspinas, A.-S., Durand, E. Y., & Slatkin, M. (2012) · Molecular Biology and Evolution · doi:10.1093/molbev/mss117 · Cited by 101

Genome-Wide Study of Structural Variants in Bovine Holstein, Montbéliarde and Normande Dairy Breeds

Boussaha, M., Esquerré, D., Barbieri, J., Djari, A., Pinton, A., Letaïef, R., Salin, G., Escudié, F., Roulet, A., Fritz, S., et al. (2015) · PLoS ONE · doi:10.1371/journal.pone.0135931 · Cited by 106

E-health-IoT Universe: A Review

Scarpato, N., Pieroni, A., Nunzio, L. D., & Fallucchi, F. (2017) · International Journal on Advanced Science Engineering and Information Technology · doi:10.18517/ijaseit.7.6.4467 · Cited by 102

DNA Sequencing

Dewey, F. E., Pan, S., Wheeler, M. T., Quake, S. R., & Ashley, E. A. (2012) · Circulation · doi:10.1161/circulationaha.110.972828 · Cited by 105

Personalized Pharmacogenomics Profiling Using Whole-Genome Sequencing

Mizzi, C., Peters, B. A., Mitropoulou, C., Mitropoulos, K. A., Κάτσιλα, Θ., Agarwal, M. R., van Schaik, R. H., Drmanac, R., Borg, J., & Patrinos, G. P. (2014) · Pharmacogenomics · doi:10.2217/pgs.14.102 · Cited by 100

Next Generation DNA Sequencing and the Future of Genomic Medicine

Anderson, M. W., & Schrijver, I. (2010) · Genes · doi:10.3390/genes1010038 · Cited by 105

Large-scale recent expansion of European patrilineages shown by population resequencing

Batini, C., Hallast, P., Zadik, D., Delser, P. M., Benazzo, A., Ghirotto, S., Arroyo‐Pardo, E., Cavalleri, G. L., de Knijff, P., Dupuy, B. M., et al. (2015) · Nature Communications · doi:10.1038/ncomms8152 · Cited by 101

Unraveling the Genetics of Cancer: Genome Sequencing and Beyond

Wong, K. M., Hudson, T. J., & McPherson, J. D. (2011) · Annual Review of Genomics and Human Genetics · doi:10.1146/annurev-genom-082509-141532 · Cited by 96

A unified test of linkage analysis and rare-variant association for analysis of pedigree sequence data

Hu, H., Roach, J. C., Coon, H. H., Guthery, S. L., Voelkerding, K. V., Margraf, R. L., Durtschi, J., Tavtigian, S. V., Shankaracharya, N. A., Wu, W., et al. (2014) · Nature Biotechnology · doi:10.1038/nbt.2895 · Cited by 94

High throughput DNA sequencing: The new sequencing revolution

Delseny, M., Han, B., & Hsing, Y. I. (2010) · Plant Science · doi:10.1016/j.plantsci.2010.07.019 · Cited by 102

MLLT1 YEATS domain mutations in clinically distinctive Favourable Histology Wilms tumours

Perlman, E. J., Gadd, S., Arold, S. T., Radhakrishnan, A., Gerhard, D. S., Jennings, L. J., Huff, V., Auvil, J. M. G., Davidsen, T. M., Dome, J. S., et al. (2015) · Nature Communications · doi:10.1038/ncomms10013 · Cited by 95

Comparative analysis of novel MGISEQ-2000 sequencing platform vs Illumina HiSeq 2500 for whole-genome sequencing

Korostin, D. O., Kulemin, N. A., Naumov, V. A., Belova, V., Kwon, D., & Gorbachev, A. Y. (2020) · PLoS ONE · doi:10.1371/journal.pone.0230301 · Cited by 96

Mutation of KCNJ8 in a patient with Cantú syndrome with unique vascular abnormalities – Support for the role of K(ATP) channels in this condition

Brownstein, C. A., Towne, M. C., Luquette, L. J., Harris, D. J., Marinakis, N. S., Meinecke, P., Kutsche, K., Campeau, P. M., Yu, T. W., Margulies, D. M., et al. (2013) · European Journal of Medical Genetics · doi:10.1016/j.ejmg.2013.09.009 · Cited by 96

Population genetic inference from personal genome data: impact of ancestry and admixture on human genomic variation

Kidd, J. M., Gravel, S., Byrnes, J., Moreno-Estrada, A., Musharoff, S., Bryc, K., Degenhardt, J. D., Brisbin, A., Sheth, V., Chen, R., et al. (2012) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2012.08.025 · Cited by 95

Computational methods for detecting copy number variations in cancer genome using next generation sequencing: principles and challenges

Liu, B., Morrison, C. D., Johnson, C. S., Trump, D. L., Qin, M., Conroy, J., Wang, J., & Liu, S. (2013) · Oncotarget · doi:10.18632/oncotarget.1537 · Cited by 96

Population genomics of human adaptation

Lachance, J., & Tishkoff, S. A. (2013) · Annual Review of Ecology, Evolution, and Systematics · doi:10.1146/annurev-ecolsys-110512-135833 · Cited by 95

Whole-genome DNA/RNA sequencing identifies truncating mutations in RBCK1 in a novel Mendelian disease with neuromuscular and cardiac involvement

Wang, K., Kim, C., Bradfield, J. P., Guo, Y., Toskala, E. M., Otieno, F. G., Hou, C., Thomas, K., Cardinale, C. J., Lyon, G. J., et al. (2013) · Genome Medicine · doi:10.1186/gm471 · Cited by 94

Chad Genetic Diversity Reveals an African History Marked by Multiple Holocene Eurasian Migrations

Haber, M., Mezzavilla, M., Bergström, A., Prado-Martinez, J., Hallast, P., Saif-Ali, R., Al‐Habori, M., Dedoussis, G. V., Zeggini, E., Blue-Smith, J., et al. (2016) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2016.10.012 · Cited by 95

Advances in the diagnosis of key gastrointestinal nematode infections of livestock, with an emphasis on small ruminants

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Coverage Bias and Sensitivity of Variant Calling for Four Whole-genome Sequencing Technologies

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