تعدد أشكال النوكليوتيدات المفردة (Arabic Wikipedia)

Analysis of information sources in references of the Wikipedia article "تعدد أشكال النوكليوتيدات المفردة" in Arabic language version.

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75nih.gov

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52doi.org

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15web.archive.org

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12harvard.edu

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1nature.com

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1bond.edu.au

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Nachman, Michael W. (2001). "Single nucleotide polymorphisms and recombination rate in humans". Trends in genetics. ج. 17 ع. 9: 481–485. DOI:10.1016/S0168-9525(01)02409-X. PMID:11525814.
"Single nucleotide polymorphisms and recombination rate in humans". Trends in Genetics. ج. 17 ع. 9: 481–5. سبتمبر 2001. DOI:10.1016/S0168-9525(01)02409-X. PMID:11525814.
"Clinical relevance of genetic polymorphisms in the human CYP2C subfamily". British Journal of Clinical Pharmacology. ج. 52 ع. 4: 349–55. أكتوبر 2001. DOI:10.1046/j.0306-5251.2001.01499.x. PMC:2014584. PMID:11678778.

bond.edu.au

epublications.bond.edu.au

"Forensically relevant SNP classes". BioTechniques. ج. 44 ع. 5: 603–8, 610. أبريل 2008. DOI:10.2144/000112806. PMID:18474034. مؤرشف من الأصل في 2011-04-13.

doi.org

Barreiro LB؛ Laval G؛ Quach H؛ Patin E؛ Quintana-Murci L. (2008). "Natural selection has driven population differentiation in modern humans". Nature Genetics. ج. 40 ع. 3: 340–345. DOI:10.1038/ng.78. PMID:18246066.
Nachman, Michael W. (2001). "Single nucleotide polymorphisms and recombination rate in humans". Trends in genetics. ج. 17 ع. 9: 481–485. DOI:10.1016/S0168-9525(01)02409-X. PMID:11525814.
"A specific chemical difference between the globins of normal human and sickle-cell anaemia haemoglobin". Nature. ج. 178 ع. 4537: 792–4. أكتوبر 1956. Bibcode:1956Natur.178..792I. DOI:10.1038/178792a0. PMID:13369537.
"beta 0 thalassemia, a nonsense mutation in man". Proceedings of the National Academy of Sciences of the United States of America. ج. 76 ع. 6: 2886–9. يونيو 1979. Bibcode:1979PNAS...76.2886C. DOI:10.1073/pnas.76.6.2886. PMC:383714. PMID:88735.
"APOE and neuroenergetics: an emerging paradigm in Alzheimer's disease". Neurobiology of Aging. ج. 34 ع. 4: 1007–17. أبريل 2013. DOI:10.1016/j.neurobiolaging.2012.10.011. PMC:3545040. PMID:23159550.
"Haplotype block partitioning and tag SNP selection using genotype data and their applications to association studies". Genome Research. ج. 14 ع. 5: 908–16. مايو 2004. DOI:10.1101/gr.1837404. PMC:479119. PMID:15078859.
"A global reference for human genetic variation". Nature. ج. 526 ع. 7571: 68–74. أكتوبر 2015. Bibcode:2015Natur.526...68T. DOI:10.1038/nature15393. PMC:4750478. PMID:26432245.
"Natural selection has driven population differentiation in modern humans". Nature Genetics. ج. 40 ع. 3: 340–5. مارس 2008. DOI:10.1038/ng.78. PMID:18246066.
"Single nucleotide polymorphisms and recombination rate in humans". Trends in Genetics. ج. 17 ع. 9: 481–5. سبتمبر 2001. DOI:10.1016/S0168-9525(01)02409-X. PMID:11525814.
"Heterogeneous distribution of SNPs in the human genome: microsatellites as predictors of nucleotide diversity and divergence". Genomics. ج. 95 ع. 3: 151–9. مارس 2010. DOI:10.1016/j.ygeno.2009.12.003. PMID:20026267.
"Enrichment of Minor Alleles of Common SNPs and Improved Risk Prediction for Parkinson's Disease". PLOS ONE. ج. 10 ع. 7: e0133421. 24 يوليو 2015. Bibcode:2015PLoSO..1033421Z. DOI:10.1371/journal.pone.0133421. PMC:4514478. PMID:26207627.{{استشهاد بدورية محكمة}}: صيانة الاستشهاد: دوي مجاني غير معلم (link)
Hivert، Valentin؛ Leblois، Raphaël؛ Petit، Eric J.؛ Gautier، Mathieu؛ Vitalis، Renaud (30 يوليو 2018). "Measuring Genetic Differentiation from Pool-seq Data". Genetics. ج. 210 ع. 1: 315–330. DOI:10.1534/genetics.118.300900. ISSN:0016-6731. مؤرشف من الأصل في 2020-12-18.
Ekblom، R؛ Galindo، J (8 ديسمبر 2010). "Applications of next generation sequencing in molecular ecology of non-model organisms". Heredity. ج. 107 ع. 1: 1–15. DOI:10.1038/hdy.2010.152. ISSN:0018-067X. مؤرشف من الأصل في 2020-05-28.
Ellegren، Hans (يناير 2014). "Genome sequencing and population genomics in non-model organisms". Trends in Ecology & Evolution. ج. 29 ع. 1: 51–63. DOI:10.1016/j.tree.2013.09.008. ISSN:0169-5347. مؤرشف من الأصل في 2020-10-10.
Dorant, Yann; Benestan, Laura; Rougemont, Quentin; Normandeau, Eric; Boyle, Brian; Rochette, Rémy; Bernatchez, Louis (2019). "Comparing Pool-seq, Rapture, and GBS genotyping for inferring weak population structure: The American lobster (Homarus americanus) as a case study". Ecology and Evolution (بالإنجليزية). 9 (11): 6606–6623. DOI:10.1002/ece3.5240. ISSN:2045-7758. PMC:6580275. PMID:31236247. Archived from the original on 2020-02-12.
Vendrami، David L. J.؛ Telesca، Luca؛ Weigand، Hannah؛ Weiss، Martina؛ Fawcett، Katie؛ Lehman، Katrin؛ Clark، M. S.؛ Leese، Florian؛ McMinn، Carrie. "RAD sequencing resolves fine-scale population structure in a benthic invertebrate: implications for understanding phenotypic plasticity". Royal Society Open Science. ج. 4 ع. 2: 160548. DOI:10.1098/rsos.160548. PMC:5367306. PMID:28386419. مؤرشف من الأصل في 2020-05-27.
"Application of a high-resolution genetic map for chromosome-scale genome assembly and fine QTLs mapping of seed size and weight traits in castor bean". Scientific Reports. ج. 9 ع. 1: 11950. أغسطس 2019. Bibcode:2019NatSR...911950Y. DOI:10.1038/s41598-019-48492-8. PMC:6697702. PMID:31420567. {{استشهاد بدورية محكمة}}: الوسيط |إظهار المؤلفين=6 غير صالح (مساعدة)
"Challenges in the association of human single nucleotide polymorphism mentions with unique database identifiers". BMC Bioinformatics. 12 Suppl 4: S4. 2011. DOI:10.1186/1471-2105-12-S4-S4. PMC:3194196. PMID:21992066.{{استشهاد بدورية محكمة}}: صيانة الاستشهاد: دوي مجاني غير معلم (link)
"Forensic SNP Genotyping using Nanopore MinION Sequencing". Scientific Reports. ج. 7: 41759. فبراير 2017. Bibcode:2017NatSR...741759C. DOI:10.1038/srep41759. PMC:5290523. PMID:28155888.
"Developing a SNP panel for forensic identification of individuals". Forensic Science International. ج. 164 ع. 1: 20–32. ديسمبر 2006. DOI:10.1016/j.forsciint.2005.11.017. PMID:16360294.
"Forensically relevant SNP classes". BioTechniques. ج. 44 ع. 5: 603–8, 610. أبريل 2008. DOI:10.2144/000112806. PMID:18474034. مؤرشف من الأصل في 2011-04-13.
"Clinical relevance of genetic polymorphisms in the human CYP2C subfamily". British Journal of Clinical Pharmacology. ج. 52 ع. 4: 349–55. أكتوبر 2001. DOI:10.1046/j.0306-5251.2001.01499.x. PMC:2014584. PMID:11678778.
"Functional SNPs of the breast cancer resistance protein-therapeutic effects and inhibitor development". Cancer Letters. ج. 234 ع. 1: 73–80. مارس 2006. DOI:10.1016/j.canlet.2005.04.039. PMID:16303243.
Butler، Merlin G. (2018). "Pharmacogenetics and Psychiatric Care: A Review and Commentary". Journal of Mental Health & Clinical Psychology. ج. 2 ع. 2: 17–24. DOI:10.29245/2578-2959/2018/2.1120. PMC:6291002. PMID:30556062.
"Single-nucleotide polymorphism in genome-wide association of human population: A tool for broad spectrum service". Egyptian Journal of Medical Human Genetics. ج. 14 ع. 2: 123–134. أبريل 2013. DOI:10.1016/j.ejmhg.2012.08.001.
"SNP-SNP interactions within APOE gene influence plasma lipids in postmenopausal osteoporosis". Rheumatology International. ج. 31 ع. 3: 421–3. مارس 2011. DOI:10.1007/s00296-010-1449-7. PMID:20340021.
"DNA polymorphism adjacent to human apoprotein A-1 gene: relation to hypertriglyceridaemia". Lancet. ج. 1 ع. 8322: 444–6. فبراير 1983. DOI:10.1016/S0140-6736(83)91440-X. PMID:6131168.
"Regulatory Variants and Disease: The E-Cadherin -160C/A SNP as an Example". Molecular Biology International. ج. 2014: 967565. 2014. DOI:10.1155/2014/967565. PMC:4167656. PMID:25276428.{{استشهاد بدورية محكمة}}: صيانة الاستشهاد: دوي مجاني غير معلم (link)
"IFNL3 mRNA structure is remodeled by a functional non-coding polymorphism associated with hepatitis C virus clearance". Scientific Reports. ج. 5: 16037. نوفمبر 2015. Bibcode:2015NatSR...516037L. DOI:10.1038/srep16037. PMC:4631997. PMID:26531896.
"A "silent" polymorphism in the MDR1 gene changes substrate specificity". Science. ج. 315 ع. 5811: 525–8. يناير 2007. Bibcode:2007Sci...315..525K. DOI:10.1126/science.1135308. PMID:17185560. مؤرشف من الأصل في 2020-08-07.
"A novel homozygous p.Arg527Leu LMNA mutation in two unrelated Egyptian families causes overlapping mandibuloacral dysplasia and progeria syndrome". European Journal of Human Genetics. ج. 20 ع. 11: 1134–40. نوفمبر 2012. DOI:10.1038/ejhg.2012.77. PMC:3476705. PMID:22549407.
"CFTR mutation analysis and haplotype associations in CF patients". Molecular Genetics and Metabolism. ج. 105 ع. 2: 249–54. فبراير 2012. DOI:10.1016/j.ymgme.2011.10.013. PMC:3551260. PMID:22137130.
"Anger- and aggression-related traits are associated with polymorphisms in the 5-HT-2A gene". Journal of Affective Disorders. ج. 96 ع. 1–2: 75–81. نوفمبر 2006. DOI:10.1016/j.jad.2006.05.016. PMID:16814396.
"Factor V Leiden thrombophilia". Genetics in Medicine. ج. 13 ع. 1: 1–16. يناير 2011. DOI:10.1097/GIM.0b013e3181faa0f2. PMID:21116184.
"Genotyping of triallelic SNPs using TaqMan PCR". Molecular and Cellular Probes. ج. 21 ع. 3: 171–6. يونيو 2007. DOI:10.1016/j.mcp.2006.10.005. PMID:17161935.
"Bitter taste study in a sardinian genetic isolate supports the association of phenylthiocarbamide sensitivity to the TAS2R38 bitter receptor gene". Chemical Senses. ج. 29 ع. 8: 697–702. أكتوبر 2004. DOI:10.1093/chemse/bjh074. PMID:15466815.
"Non-synonymous polymorphisms in the FCN1 gene determine ligand-binding ability and serum levels of M-ficolin". PLOS ONE. ج. 7 ع. 11: e50585. 28 نوفمبر 2012. Bibcode:2012PLoSO...750585A. DOI:10.1371/journal.pone.0050585. PMC:3509001. PMID:23209787.{{استشهاد بدورية محكمة}}: صيانة الاستشهاد: دوي مجاني غير معلم (link)
"Common variants in mismatch repair genes associated with increased risk of sperm DNA damage and male infertility". BMC Medicine. ج. 10: 49. مايو 2012. DOI:10.1186/1741-7015-10-49. PMC:3378460. PMID:22594646.{{استشهاد بدورية محكمة}}: صيانة الاستشهاد: دوي مجاني غير معلم (link)
"Kaviar: an accessible system for testing SNV novelty". Bioinformatics. ج. 27 ع. 22: 3216–7. نوفمبر 2011. DOI:10.1093/bioinformatics/btr540. PMC:3208392. PMID:21965822.
"dbSAP: single amino-acid polymorphism database for protein variation detection". Nucleic Acids Research. ج. 45 ع. D1: D827–D832. يناير 2017. DOI:10.1093/nar/gkw1096. PMC:5210569. PMID:27903894.
"A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms". Nature. ج. 409 ع. 6822: 928–33. فبراير 2001. Bibcode:2001Natur.409..928S. DOI:10.1038/35057149. PMID:11237013.
"An SNP map of the human genome generated by reduced representation shotgun sequencing". Nature. ج. 407 ع. 6803: 513–6. سبتمبر 2000. Bibcode:2000Natur.407..513A. DOI:10.1038/35035083. PMID:11029002.
"Identification of base pairs in single-nucleotide polymorphisms by MutS protein-mediated capillary electrophoresis". Analytical Chemistry. ج. 78 ع. 6: 2035–8. مارس 2006. DOI:10.1021/ac0520386. PMID:16536443.
"Genetic identification by mass spectrometric analysis of single-nucleotide polymorphisms: ternary encoding of genotypes". Analytical Chemistry. ج. 72 ع. 14: 3298–302. يوليو 2000. DOI:10.1021/ac991390e. PMID:10939403.
"Estimation of SNP allele frequencies by SSCP analysis of pooled DNA". Single Nucleotide Polymorphisms. Methods in Molecular Biology. ج. 578. 2009. ص. 193–207. DOI:10.1007/978-1-60327-411-1_12. ISBN:978-1-60327-410-4. PMID:19768595.
"Improved measures for evolutionary conservation that exploit taxonomy distances". Nature Communications. ج. 10 ع. 1: 1556. أبريل 2019. Bibcode:2019NatCo..10.1556M. DOI:10.1038/s41467-019-09583-2. PMC:6450959. PMID:30952844.
Nawar Malhis؛ Matthew Jacobson؛ Steven J. M. Jones؛ Jörg Gsponer (2020). "LIST-S2: Taxonomy Based Sorting of Deleterious Missense Mutations Across Species". Nucleic Acids Research. ج. 48 ع. W1: W154–W161. DOI:10.1093/nar/gkaa288. PMC:7319545. PMID:32352516.
"PhyreRisk: A Dynamic Web Application to Bridge Genomics, Proteomics and 3D Structural Data to Guide Interpretation of Human Genetic Variants". Journal of Molecular Biology. ج. 431 ع. 13: 2460–2466. يونيو 2019. DOI:10.1016/j.jmb.2019.04.043. PMC:6597944. PMID:31075275. {{استشهاد بدورية محكمة}}: الوسيط |إظهار المؤلفين=6 غير صالح (مساعدة)
"Can Predicted Protein 3D Structures Provide Reliable Insights into whether Missense Variants Are Disease Associated?". Journal of Molecular Biology. ج. 431 ع. 11: 2197–2212. مايو 2019. DOI:10.1016/j.jmb.2019.04.009. PMC:6544567. PMID:30995449.

dx.doi.org

Hivert، Valentin؛ Leblois، Raphaël؛ Petit، Eric J.؛ Gautier، Mathieu؛ Vitalis، Renaud (30 يوليو 2018). "Measuring Genetic Differentiation from Pool-seq Data". Genetics. ج. 210 ع. 1: 315–330. DOI:10.1534/genetics.118.300900. ISSN:0016-6731. مؤرشف من الأصل في 2020-12-18.
Ekblom، R؛ Galindo، J (8 ديسمبر 2010). "Applications of next generation sequencing in molecular ecology of non-model organisms". Heredity. ج. 107 ع. 1: 1–15. DOI:10.1038/hdy.2010.152. ISSN:0018-067X. مؤرشف من الأصل في 2020-05-28.
Ellegren، Hans (يناير 2014). "Genome sequencing and population genomics in non-model organisms". Trends in Ecology & Evolution. ج. 29 ع. 1: 51–63. DOI:10.1016/j.tree.2013.09.008. ISSN:0169-5347. مؤرشف من الأصل في 2020-10-10.

genengnews.com

Carlson، Bruce (15 يونيو 2008). "SNPs — A Shortcut to Personalized Medicine". ماري آن ليبيرت. ج. 28 ع. 12. مؤرشف من الأصل في 2010-12-26. اطلع عليه بتاريخ 2008-07-06. (subtitle) Medical applications are where the market's growth is expected

genomicscomputbiol.org

"View of SNPViz - Visualization of SNPs in proteins". genomicscomputbiol.org (بالإنجليزية الأمريكية). Archived from the original on 2020-08-07. Retrieved 2018-10-20.

harvard.edu

ui.adsabs.harvard.edu

"A specific chemical difference between the globins of normal human and sickle-cell anaemia haemoglobin". Nature. ج. 178 ع. 4537: 792–4. أكتوبر 1956. Bibcode:1956Natur.178..792I. DOI:10.1038/178792a0. PMID:13369537.
"beta 0 thalassemia, a nonsense mutation in man". Proceedings of the National Academy of Sciences of the United States of America. ج. 76 ع. 6: 2886–9. يونيو 1979. Bibcode:1979PNAS...76.2886C. DOI:10.1073/pnas.76.6.2886. PMC:383714. PMID:88735.
"A global reference for human genetic variation". Nature. ج. 526 ع. 7571: 68–74. أكتوبر 2015. Bibcode:2015Natur.526...68T. DOI:10.1038/nature15393. PMC:4750478. PMID:26432245.
"Enrichment of Minor Alleles of Common SNPs and Improved Risk Prediction for Parkinson's Disease". PLOS ONE. ج. 10 ع. 7: e0133421. 24 يوليو 2015. Bibcode:2015PLoSO..1033421Z. DOI:10.1371/journal.pone.0133421. PMC:4514478. PMID:26207627.{{استشهاد بدورية محكمة}}: صيانة الاستشهاد: دوي مجاني غير معلم (link)
"Application of a high-resolution genetic map for chromosome-scale genome assembly and fine QTLs mapping of seed size and weight traits in castor bean". Scientific Reports. ج. 9 ع. 1: 11950. أغسطس 2019. Bibcode:2019NatSR...911950Y. DOI:10.1038/s41598-019-48492-8. PMC:6697702. PMID:31420567. {{استشهاد بدورية محكمة}}: الوسيط |إظهار المؤلفين=6 غير صالح (مساعدة)
"Forensic SNP Genotyping using Nanopore MinION Sequencing". Scientific Reports. ج. 7: 41759. فبراير 2017. Bibcode:2017NatSR...741759C. DOI:10.1038/srep41759. PMC:5290523. PMID:28155888.
"IFNL3 mRNA structure is remodeled by a functional non-coding polymorphism associated with hepatitis C virus clearance". Scientific Reports. ج. 5: 16037. نوفمبر 2015. Bibcode:2015NatSR...516037L. DOI:10.1038/srep16037. PMC:4631997. PMID:26531896.
"A "silent" polymorphism in the MDR1 gene changes substrate specificity". Science. ج. 315 ع. 5811: 525–8. يناير 2007. Bibcode:2007Sci...315..525K. DOI:10.1126/science.1135308. PMID:17185560. مؤرشف من الأصل في 2020-08-07.
"Non-synonymous polymorphisms in the FCN1 gene determine ligand-binding ability and serum levels of M-ficolin". PLOS ONE. ج. 7 ع. 11: e50585. 28 نوفمبر 2012. Bibcode:2012PLoSO...750585A. DOI:10.1371/journal.pone.0050585. PMC:3509001. PMID:23209787.{{استشهاد بدورية محكمة}}: صيانة الاستشهاد: دوي مجاني غير معلم (link)
"A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms". Nature. ج. 409 ع. 6822: 928–33. فبراير 2001. Bibcode:2001Natur.409..928S. DOI:10.1038/35057149. PMID:11237013.
"An SNP map of the human genome generated by reduced representation shotgun sequencing". Nature. ج. 407 ع. 6803: 513–6. سبتمبر 2000. Bibcode:2000Natur.407..513A. DOI:10.1038/35035083. PMID:11029002.
"Improved measures for evolutionary conservation that exploit taxonomy distances". Nature Communications. ج. 10 ع. 1: 1556. أبريل 2019. Bibcode:2019NatCo..10.1556M. DOI:10.1038/s41467-019-09583-2. PMC:6450959. PMID:30952844.

iso.org

ISO - ISO 20395:2019 - Biotechnology — Requirements for evaluating the performance of quantification methods for nucleic acid target sequences — qPCR and dPCR نسخة محفوظة 2020-11-01 على موقع واي باك مشين.

nature.com

"single-nucleotide polymorphism / SNP | Learn Science at Scitable". www.nature.com. مؤرشف من الأصل في 2015-11-10. اطلع عليه بتاريخ 2015-11-13.

nih.gov

pubmed.ncbi.nlm.nih.gov

Barreiro LB؛ Laval G؛ Quach H؛ Patin E؛ Quintana-Murci L. (2008). "Natural selection has driven population differentiation in modern humans". Nature Genetics. ج. 40 ع. 3: 340–345. DOI:10.1038/ng.78. PMID:18246066.
Nachman, Michael W. (2001). "Single nucleotide polymorphisms and recombination rate in humans". Trends in genetics. ج. 17 ع. 9: 481–485. DOI:10.1016/S0168-9525(01)02409-X. PMID:11525814.
"A specific chemical difference between the globins of normal human and sickle-cell anaemia haemoglobin". Nature. ج. 178 ع. 4537: 792–4. أكتوبر 1956. Bibcode:1956Natur.178..792I. DOI:10.1038/178792a0. PMID:13369537.
"beta 0 thalassemia, a nonsense mutation in man". Proceedings of the National Academy of Sciences of the United States of America. ج. 76 ع. 6: 2886–9. يونيو 1979. Bibcode:1979PNAS...76.2886C. DOI:10.1073/pnas.76.6.2886. PMC:383714. PMID:88735.
"Cystic fibrosis patients bearing both the common missense mutation Gly----Asp at codon 551 and the delta F508 mutation are clinically indistinguishable from delta F508 homozygotes, except for decreased risk of meconium ileus". American Journal of Human Genetics. ج. 51 ع. 2: 245–50. أغسطس 1992. PMC:1682672. PMID:1379413.
"APOE and neuroenergetics: an emerging paradigm in Alzheimer's disease". Neurobiology of Aging. ج. 34 ع. 4: 1007–17. أبريل 2013. DOI:10.1016/j.neurobiolaging.2012.10.011. PMC:3545040. PMID:23159550.
"Haplotype block partitioning and tag SNP selection using genotype data and their applications to association studies". Genome Research. ج. 14 ع. 5: 908–16. مايو 2004. DOI:10.1101/gr.1837404. PMC:479119. PMID:15078859.
"A global reference for human genetic variation". Nature. ج. 526 ع. 7571: 68–74. أكتوبر 2015. Bibcode:2015Natur.526...68T. DOI:10.1038/nature15393. PMC:4750478. PMID:26432245.
"Natural selection has driven population differentiation in modern humans". Nature Genetics. ج. 40 ع. 3: 340–5. مارس 2008. DOI:10.1038/ng.78. PMID:18246066.
"Single nucleotide polymorphisms and recombination rate in humans". Trends in Genetics. ج. 17 ع. 9: 481–5. سبتمبر 2001. DOI:10.1016/S0168-9525(01)02409-X. PMID:11525814.
"Heterogeneous distribution of SNPs in the human genome: microsatellites as predictors of nucleotide diversity and divergence". Genomics. ج. 95 ع. 3: 151–9. مارس 2010. DOI:10.1016/j.ygeno.2009.12.003. PMID:20026267.
"Enrichment of Minor Alleles of Common SNPs and Improved Risk Prediction for Parkinson's Disease". PLOS ONE. ج. 10 ع. 7: e0133421. 24 يوليو 2015. Bibcode:2015PLoSO..1033421Z. DOI:10.1371/journal.pone.0133421. PMC:4514478. PMID:26207627.{{استشهاد بدورية محكمة}}: صيانة الاستشهاد: دوي مجاني غير معلم (link)
Dorant, Yann; Benestan, Laura; Rougemont, Quentin; Normandeau, Eric; Boyle, Brian; Rochette, Rémy; Bernatchez, Louis (2019). "Comparing Pool-seq, Rapture, and GBS genotyping for inferring weak population structure: The American lobster (Homarus americanus) as a case study". Ecology and Evolution (بالإنجليزية). 9 (11): 6606–6623. DOI:10.1002/ece3.5240. ISSN:2045-7758. PMC:6580275. PMID:31236247. Archived from the original on 2020-02-12.
Vendrami، David L. J.؛ Telesca، Luca؛ Weigand، Hannah؛ Weiss، Martina؛ Fawcett، Katie؛ Lehman، Katrin؛ Clark، M. S.؛ Leese، Florian؛ McMinn، Carrie. "RAD sequencing resolves fine-scale population structure in a benthic invertebrate: implications for understanding phenotypic plasticity". Royal Society Open Science. ج. 4 ع. 2: 160548. DOI:10.1098/rsos.160548. PMC:5367306. PMID:28386419. مؤرشف من الأصل في 2020-05-27.
"Application of a high-resolution genetic map for chromosome-scale genome assembly and fine QTLs mapping of seed size and weight traits in castor bean". Scientific Reports. ج. 9 ع. 1: 11950. أغسطس 2019. Bibcode:2019NatSR...911950Y. DOI:10.1038/s41598-019-48492-8. PMC:6697702. PMID:31420567. {{استشهاد بدورية محكمة}}: الوسيط |إظهار المؤلفين=6 غير صالح (مساعدة)
"Challenges in the association of human single nucleotide polymorphism mentions with unique database identifiers". BMC Bioinformatics. 12 Suppl 4: S4. 2011. DOI:10.1186/1471-2105-12-S4-S4. PMC:3194196. PMID:21992066.{{استشهاد بدورية محكمة}}: صيانة الاستشهاد: دوي مجاني غير معلم (link)
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qiagenbioinformatics.com

resources.qiagenbioinformatics.com

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ISO - ISO 20395:2019 - Biotechnology — Requirements for evaluating the performance of quantification methods for nucleic acid target sequences — qPCR and dPCR نسخة محفوظة 2020-11-01 على موقع واي باك مشين.
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wiley.com

onlinelibrary.wiley.com

Dorant, Yann; Benestan, Laura; Rougemont, Quentin; Normandeau, Eric; Boyle, Brian; Rochette, Rémy; Bernatchez, Louis (2019). "Comparing Pool-seq, Rapture, and GBS genotyping for inferring weak population structure: The American lobster (Homarus americanus) as a case study". Ecology and Evolution (بالإنجليزية). 9 (11): 6606–6623. DOI:10.1002/ece3.5240. ISSN:2045-7758. PMC:6580275. PMID:31236247. Archived from the original on 2020-02-12.

worldcat.org

Hivert، Valentin؛ Leblois، Raphaël؛ Petit، Eric J.؛ Gautier، Mathieu؛ Vitalis، Renaud (30 يوليو 2018). "Measuring Genetic Differentiation from Pool-seq Data". Genetics. ج. 210 ع. 1: 315–330. DOI:10.1534/genetics.118.300900. ISSN:0016-6731. مؤرشف من الأصل في 2020-12-18.
Ekblom، R؛ Galindo، J (8 ديسمبر 2010). "Applications of next generation sequencing in molecular ecology of non-model organisms". Heredity. ج. 107 ع. 1: 1–15. DOI:10.1038/hdy.2010.152. ISSN:0018-067X. مؤرشف من الأصل في 2020-05-28.
Ellegren، Hans (يناير 2014). "Genome sequencing and population genomics in non-model organisms". Trends in Ecology & Evolution. ج. 29 ع. 1: 51–63. DOI:10.1016/j.tree.2013.09.008. ISSN:0169-5347. مؤرشف من الأصل في 2020-10-10.
Dorant, Yann; Benestan, Laura; Rougemont, Quentin; Normandeau, Eric; Boyle, Brian; Rochette, Rémy; Bernatchez, Louis (2019). "Comparing Pool-seq, Rapture, and GBS genotyping for inferring weak population structure: The American lobster (Homarus americanus) as a case study". Ecology and Evolution (بالإنجليزية). 9 (11): 6606–6623. DOI:10.1002/ece3.5240. ISSN:2045-7758. PMC:6580275. PMID:31236247. Archived from the original on 2020-02-12.

zenodo.org

"A "silent" polymorphism in the MDR1 gene changes substrate specificity". Science. ج. 315 ع. 5811: 525–8. يناير 2007. Bibcode:2007Sci...315..525K. DOI:10.1126/science.1135308. PMID:17185560. مؤرشف من الأصل في 2020-08-07.