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Genetic marker

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and/or insertion. Markers can exhibit two modes of inheritance, i.e. dominant/recessive or co-dominant. If the genetic pattern of homo-zygotes can be distinguished from that of hetero-zygotes, then a marker is said to be co-dominant. Generally co-dominant markers are more informative than the dominant markers.
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Genetic markers have also been used to measure the genomic response to selection in livestock. Natural and artificial selection leads to a change in the genetic makeup of the cell. The presence of different alleles due to a distorted segregation at the genetic markers is indicative of the difference
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Molecular genetic markers can be divided into two classes: a) biochemical markers which detect variation at the gene product level such as changes in proteins and amino acids and b) molecular markers which detect variation at the DNA level such as nucleotide changes: deletion, duplication, inversion
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was limited to identifying organisms by traditional phenotypes markers. This included genes that encoded easily observable characteristics, such as blood types or seed shapes. The insufficient number of these types of characteristics in several organisms limited the possible mapping efforts. This
290:. With the aid of genetic markers, researchers were able to provide conclusive evidence that the cancerous tumor cell evolved into a transmissible parasite. Furthermore, molecular genetic markers were used to resolve the issue of natural transmission, the breed of origin ( 214:). It is known that pieces of DNA that lie near each other on a chromosome tend to be inherited together. This property enables the use of a marker, which can then be used to determine the precise inheritance pattern of the gene that has not yet been exactly localized. 39:. It can be described as a variation (which may arise due to mutation or alteration in the genomic loci) that can be observed. A genetic marker may be a short DNA sequence, such as a sequence surrounding a single base-pair change ( 375:
Mehta, Sahil; Singh, Baljinder; Dhakate, Priyanka; Rahman, Mehzabin; Islam, Muhammad Aminul (2019). "5 Rice, Marker-Assisted Breeding, and Disease Resistance". In Wani, Shabir Hussain (ed.).
286:) was. Many researchers hypothesized that virus like particles were responsible for transforming the cell, while others thought that the cell itself was able to infect other canines as an 529: 152: 60:
prompted the development of gene markers, which could identify genetic characteristics that are not readily observable in organisms (such as protein variation).
562: 540: 545:. AMS (Bioversity's Regional Office for the Americas), CIRAD, GCP, IPGRI, M.S. Swaminathan Research Foundation. p. 85. Archived from 81: 166: 116: 102: 518: 95: 435: 411: 392: 356: 322: 283: 88: 454:, Kim SY, Fassati A, Weiss RA. Clonal origin and evolution of a transmissible cancer. Cell. 2006 Aug 11;126(3):477-87. 594: 464:
Gomez-Raya L, Olsen HG, Lingaas F, Klungland H, Våge DI, Olsaker I, Talle SB, Aasland M, Lien S (November 2002).
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do not provide any information. Detection of the marker can be direct by RNA sequencing, or indirect using
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are RFLP, AFLP, RAPD, SSR. They can be used to create genetic maps of whatever organism is being studied.
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Disease Resistance in Crop Plants : Molecular, Genetic and Genomic Perspectives
485: 477: 312: 249: 226: 481: 466:"The use of genetic markers to measure genomic response to selection in livestock" 534:. IPGRI, Rome, Italy and Institute for Genetic Diversity, Ithaca, New York, USA. 523:. IPGRI, Rome, Italy and Institute for Genetic Diversity, Ithaca, New York, USA. 402: 603: 291: 272: 44: 427:
Genetic Mapping and Marker Assisted Selection: Basics, Practice and Benefits
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Genetic markers have to be easily identifiable, associated with a specific
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Genetic markers can be used to study the relationship between an
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between individuals or populations. Uniparental markers (on
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Gene or DNA sequence with a known location on a chromosome
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There was a debate over what the transmissible agent of
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DNA) are studied for assessing maternal or paternal
538: 370: 368: 346: 76:Some commonly used types of genetic markers are: 601: 561:Spooner D, van Treuren R, de Vicente MC (2005). 527: 516: 567:. CGN, IPGRI, USDA. p. 126. Archived from 365: 298:between selected and non-selected livestock. 35:that can be used to identify individuals or 457: 417: 531:Molecular Marker Learning Modules – Vol. 2 520:Molecular Marker Learning Modules – Vol. 1 564:Molecular markers for genebank management 489: 82:Restriction fragment length polymorphism 72:SFP discovery principle for gene probing 67: 167:Restriction site associated DNA markers 117:Single-strand conformation polymorphism 103:Random amplification of polymorphic DNA 602: 267:Some of the methods used to study the 96:Amplified fragment length polymorphism 323:Eukaryotic chromosome fine structure 294:), and the age of the canine tumor. 542:Molecular Markers for Allele Mining 539:de Vicente C, Glaszmann JC (2006). 424:N Manikanda Boopathi (2012-12-12). 284:canine transmissible venereal tumor 245:markers are used for all ancestry. 89:Simple sequence length polymorphism 13: 510: 14: 636: 583: 347:Benjamin A. Pierce (2013-12-27). 202:cause (for example, a particular 588: 217:Genetic markers are employed in 528:de Vicente C, Fulton T (2004). 517:de Vicente C, Fulton T (2003). 349:Genetics: A Conceptual Approach 444: 340: 139:Single nucleotide polymorphism 41:single nucleotide polymorphism 1: 333: 110:Variable number tandem repeat 50: 210:that results in a defective 43:, SNP), or a long one, like 7: 482:10.1093/genetics/162.3.1381 387:. pp. 83–112/xii+307. 301: 160:Diversity Arrays Technology 153:Single feature polymorphism 31:with a known location on a 10: 641: 219:genealogical DNA testing 63: 328:Repeated sequence (DNA) 189: 351:. Macmillan Learning. 132:Simple sequence repeat 73: 597:at Wikimedia Commons 179:Sequence-tagged sites 71: 615:Genomics techniques 610:Genetics techniques 146:Short tandem repeat 130:polymorphism, (or 74: 625:Molecular biology 593:Media related to 437:978-81-322-0958-4 412:978-3-030-20728-1 394:978-3-030-20727-4 381:Cham, Switzerland 358:978-1-4641-0946-1 223:genetic genealogy 196:inherited disease 632: 592: 579: 577: 576: 557: 555: 554: 535: 524: 504: 503: 493: 461: 455: 448: 442: 441: 421: 415: 406: 372: 363: 362: 344: 313:Molecular marker 227:genetic distance 176: 175: 165:RAD markers (or 126: 125: 55:For many years, 640: 639: 635: 634: 633: 631: 630: 629: 600: 599: 595:Genetic markers 586: 574: 572: 552: 550: 513: 511:Further reading 508: 507: 462: 458: 449: 445: 438: 422: 418: 395: 373: 366: 359: 345: 341: 336: 304: 192: 173: 172: 123: 122: 66: 53: 17: 12: 11: 5: 638: 628: 627: 622: 617: 612: 585: 584:External links 582: 581: 580: 558: 536: 525: 512: 509: 506: 505: 456: 443: 436: 416: 393: 364: 357: 338: 337: 335: 332: 331: 330: 325: 320: 315: 310: 303: 300: 191: 188: 183: 182: 170: 163: 156: 149: 142: 135: 128:Microsatellite 120: 113: 106: 99: 92: 85: 65: 62: 52: 49: 45:minisatellites 21:genetic marker 15: 9: 6: 4: 3: 2: 637: 626: 623: 621: 618: 616: 613: 611: 608: 607: 605: 598: 596: 591: 571:on 2008-05-03 570: 566: 565: 559: 549:on 2007-12-04 548: 544: 543: 537: 533: 532: 526: 522: 521: 515: 514: 501: 497: 492: 487: 483: 479: 476:(3): 1381–8. 475: 471: 467: 460: 453: 447: 439: 433: 429: 428: 420: 413: 409: 404: 400: 396: 390: 386: 382: 378: 371: 369: 360: 354: 350: 343: 339: 329: 326: 324: 321: 319: 316: 314: 311: 309: 306: 305: 299: 295: 293: 292:phylogenetics 289: 285: 281: 276: 274: 273:phylogenetics 270: 265: 263: 259: 255: 252:, and highly 251: 246: 244: 240: 236: 235:Y chromosomal 232: 231:mitochondrial 228: 225:to determine 224: 220: 215: 213: 209: 205: 201: 197: 187: 180: 171: 168: 164: 161: 157: 154: 150: 147: 143: 140: 136: 133: 129: 121: 118: 114: 111: 107: 104: 100: 97: 93: 90: 86: 83: 79: 78: 77: 70: 61: 58: 48: 46: 42: 38: 34: 30: 26: 22: 587: 573:. 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Retrieved 547:the original 541: 530: 519: 473: 469: 459: 452:Pritchard JK 446: 426: 419: 376: 348: 342: 296: 277: 266: 247: 216: 193: 184: 75: 57:gene mapping 54: 29:DNA sequence 20: 18: 318:DNA marking 308:Marker gene 258:homozygotes 254:polymorphic 604:Categories 575:2007-12-12 553:2007-12-12 450:Murgia C, 403:1110184027 334:References 256:, because 51:Background 33:chromosome 288:allograft 262:allozymes 243:Autosomal 158:DArT (or 115:SSCP (or 108:VNTR (or 101:RAPD (or 94:AFLP (or 87:SSLP (or 80:RFLP (or 500:12454081 470:Genetics 385:Springer 302:See also 239:lineages 204:mutation 198:and its 151:SFP (or 144:STR (or 137:SNP (or 491:1462338 212:protein 200:genetic 177:(using 37:species 498:  488:  434:  410:  401:  391:  355:  269:genome 250:locus 206:of a 64:Types 23:is a 496:PMID 432:ISBN 408:ISBN 399:OCLC 389:ISBN 353:ISBN 280:CTVT 221:for 208:gene 190:Uses 25:gene 620:DNA 486:PMC 478:doi 474:162 271:or 233:or 174:STS 124:SSR 27:or 606:: 494:. 484:. 472:. 468:. 397:. 383:: 379:. 367:^ 264:. 241:. 47:. 19:A 578:. 556:. 502:. 480:: 440:. 414:. 405:. 361:. 282:( 181:) 169:) 162:) 155:) 148:) 141:) 134:) 119:) 112:) 105:) 98:) 91:) 84:)

Index

gene
DNA sequence
chromosome
species
single nucleotide polymorphism
minisatellites
gene mapping

Restriction fragment length polymorphism
Simple sequence length polymorphism
Amplified fragment length polymorphism
Random amplification of polymorphic DNA
Variable number tandem repeat
Single-strand conformation polymorphism
Microsatellite
Simple sequence repeat
Single nucleotide polymorphism
Short tandem repeat
Single feature polymorphism
Diversity Arrays Technology
Restriction site associated DNA markers
Sequence-tagged sites
inherited disease
genetic
mutation
gene
protein
genealogical DNA testing
genetic genealogy
genetic distance

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