最新国产精品剧情在线SS,中文无码肉感爆乳在线观看,JAPAN日本人妻熟老太,成年在线观看免费人视频

文章詳情

Coriell Institute|NA12878 人類(lèi)基因組DNA標(biāo)準(zhǔn)品

日期:2025-07-09 17:05
瀏覽次數(shù):2599
摘要:Coriell Institute|NA12878 人類(lèi)基因組DNA標(biāo)準(zhǔn)品

知識(shí)庫(kù) NIGMS人類(lèi)遺傳細(xì)胞庫(kù)
子集合 CEPH 
Repository Linkage Families 
Pharmacogenetics 
PIGI同意樣本
數(shù)量 50微克
定量方法 請(qǐng)參閱我們的常見(jiàn)問(wèn)題
活檢來(lái)源 外周靜脈
細(xì)胞類(lèi)型 B淋|巴細(xì)胞
組織類(lèi)型 血液
轉(zhuǎn)化 愛(ài)潑斯坦 - 巴爾病毒
種族 高加索
種族 猶他州/ MORMON
出生國(guó)家 美國(guó)
家庭成員 2
與Proband的關(guān)系 母親
確認(rèn) 臨床總結(jié)/病史
ISCN 46,XX [23] .arr [hg19] 9p13.1(38,787,480-40,911,212)x3
種類(lèi) Homo  sapiens
通用名稱 人的
備注 母親; 供體受試者在CYP2C19基因(CYP2C19 * 2)的外顯子5中的核苷酸681處具有單個(gè)bp(G至A)轉(zhuǎn)變,其產(chǎn)生異常剪接位點(diǎn)。該變化改變了mRNA的閱讀框架,從氨基酸215開(kāi)始,并在下游產(chǎn)生20個(gè)氨基酸的過(guò)早終止密碼子,產(chǎn)生截短的無(wú)功能蛋白質(zhì)。由于異常剪接位點(diǎn),在外顯子5開(kāi)始時(shí)(從bp 643到bp 682)發(fā)生40bp的缺失,導(dǎo)致氨基酸215到227的缺失。截短的蛋白質(zhì)具有234個(gè)氨基酸并且將是催化失活的因?yàn)樗狈ρt素結(jié)合區(qū)域。

原產(chǎn)地物種的鑒定 核苷磷酸化酶,葡萄糖-6-磷酸脫氫酶和乳酸脫氫酶同工酶電泳確認(rèn)的原產(chǎn)地種類(lèi)
備注 母親; 供體受試者在CYP2C19基因(CYP2C19 * 2)的外顯子5中的核苷酸681處具有單個(gè)bp(G至A)轉(zhuǎn)變,其產(chǎn)生異常剪接位點(diǎn)。該變化改變了mRNA的閱讀框架,從氨基酸215開(kāi)始,并在下游產(chǎn)生20個(gè)氨基酸的過(guò)早終止密碼子,產(chǎn)生截短的無(wú)功能蛋白質(zhì)。由于異常剪接位點(diǎn),在外顯子5開(kāi)始時(shí)(從bp 643到bp 682)發(fā)生40bp的缺失,導(dǎo)致氨基酸215到227的缺失。截短的蛋白質(zhì)具有234個(gè)氨基酸并且將是催化失活的因?yàn)樗狈ρt素結(jié)合區(qū)域。
Brocard M,Khasnis S,Wood CD,Shannon-Lowe C,West MJ,Pumilio指導(dǎo)去腺苷酸化相關(guān)的轉(zhuǎn)錄抑制細(xì)胞周期蛋白依賴性激酶1活化劑RGC-32核酸研究:2018
PubMed ID:29385536
 
Blombery P,Jones K,Doig K,Ryland G,McBean M,Thompson E,Yannakou CK,Westerman D,敏感NPM1突變定量急性髓細(xì)胞白血病使用Ultradeep新一代測(cè)序在診斷實(shí)驗(yàn)室病理學(xué)和實(shí)驗(yàn)室醫(yī)學(xué)檔案:2018年
PubMed ID:29425073
 
Velasco G,Grillo G,Touleimat N,F(xiàn)erry L,Ivkovic I,Ribierre F,Deleuze JF,Chantalat S,Picard C,F(xiàn)rancastel C,ICF患者的比較甲基化組分析鑒定了需要ZBTB24,CDCA7和HELLS的甲基化狀態(tài)的異染色質(zhì)基因座人類(lèi)分子遺傳學(xué):2018
PubMed ID:29659838
 
Zhang M,Ngampeerapong C,Redin D,Ahmadian A,Sychugov I,Linnros J,Thermophoresis-Controlled Size-Dependent DNA Translocation through a Nanopores ACS nano12:4574-4582 2018
PubMed ID:29648793
 
Preissl S,F(xiàn)ang R,Huang H,Zhao Y,Raviram R,Gorkin DU,Zhang Y,Sos BC,Afzal V,Dickel DE,Kuan S,Visel A,Pennacchio LA,Zhang K,Ren B,Single-nucleus analysis of在發(fā)育中的小鼠前腦中可獲得的染色質(zhì)揭示細(xì)胞類(lèi)型特異性轉(zhuǎn)錄調(diào)節(jié)Nature Neuroscience21:432-439 2017
PubMed ID:29434377
 
Lee JEA,Li N,Rowley SM,Cheasley D,Zethoven M,McInerny S,Gorringe KL,James PA,Campbell IG,PALB2相關(guān)乳腺癌的分子分析The Journal of pathology 21:432-439 2017
PubMed ID:29431189
 
Doig KD,Ellul J,F(xiàn)ellowes A,Thompson ER,Ryland G,Blombery P,Papenfuss AT,F(xiàn)ox SB,Canary:用于臨床擴(kuò)增子測(cè)定的原子管道BMC bioinformatics18:555 2017
PubMed ID:29246107
 
Trost B,Walker S,Wang Z,Thiruvahindrapuram B,MacDonald JR,Sung WWL,Pereira SL,Whitney J,Chan AJS,Pellecchia G,Reuter MS,Lok S,Yuen RKC,Marshall CR,Merico D,Scherer SW,A Comprehensive基于讀深度的全基因組序列數(shù)據(jù)拷貝數(shù)變異鑒定的工作流程美國(guó)人類(lèi)遺傳學(xué)雜志102:142-155 2017
PubMed ID:29304372
 
Numanagic I,Malikic S,F(xiàn)ord M,Qin X,Toji L,Radovich M,Skaar TC,Pratt VM,Berger B,Scherer S,Sahinalp SC,Allelic分解和高度多態(tài)性和結(jié)構(gòu)變異基因的精|確基因分型Nature communications9:828 2017
PubMed ID:29483503
 
Becker T,Lee WP,Leone J,Zhu Q,Zhang C,Liu S,Sargent J,Shanker K,Mil-Homens A,Cerveira E,Ryan M,Cha J,Navarro FCP,Galeev T,Gerstein M,Mills RE, Shin DG,Lee C,Malhotra A,F(xiàn)usorSV:一種*|佳組合多種結(jié)構(gòu)變異檢測(cè)方法數(shù)據(jù)的算法Genome biology19:38 2017
PubMed ID:29559002
 
Shigemizu D,Miya F,Akiyama S,Okuda S,Boroevich KA,F(xiàn)ujimoto A,Nakagawa H,Ozaki K,Niida S,Kanemura Y,Okamoto N,Saitoh S,Kato M,Yamasaki M,Matsunaga T,Mutai H,Kosaki K ,Tsunoda T,IMSindel:一種精|確的中等尺寸插入缺失檢測(cè)工具,包括從頭組裝和缺口全局局部對(duì)齊以及分離讀取分析科學(xué)報(bào)告8:5608 2017
PubMed ID:29618752
 
Mulqueen RM,Pokholok D,Norberg SJ,Torkenczy KA,F(xiàn)ields AJ,Sun D,Sinnamon JR,Shendure J,Trapnell C,O'Roak BJ,Xia Z,Steemers FJ,Adey AC,高度可擴(kuò)展的DNA甲基化配置文件細(xì)胞Nature biotechnology36:428-431 2017
PubMed ID:29644997
 
Soukupova J,Zemankova P,Lhotova K,Janatova M,Borecka M,Stolarova L,Lhota F,F(xiàn)oretova L,Machackova E,Stranecky V,Tavandzis S,Kleiblova P,Vocka M,Hartmannova H,Hodanova K,Kmoch S,Kleibl Z,驗(yàn)證CZECANCA(CZEch CAncer paNel for Clinical Application)用于基于NGS的遺傳性癌癥綜合征分析PloS one13:e0195761 2017
PubMed ID:29649263
 
Kamps-Hughes N,McUsic A,Kurihara L,Harkins TT,Pal P,Ray C,Ionescu-Zanetti C,ERASE-Seq:利用重復(fù)測(cè)量來(lái)增強(qiáng)NGS數(shù)據(jù)中的超低頻變異檢測(cè)PloS one13:e0195272 2017
PubMed ID:29630678
 
Garieri M1,2,3,Delaneau O1,2,3,Santoni F1,4,魚(yú)RJ1,Mull D1,Carninci P5,Dermitzakis ET1,2,3,Antonarakis SE1,2,4,A6堡壘。,遺傳變異對(duì)啟動(dòng)子使用和增強(qiáng)子活性的影響。Nat Commun8(1):1358 2017
PubMed ID:29116076
 
Pratt VM,Everts RE,Aggarwal P,Beyer BN,Broeckel U,Epstein-Baak R,Hujsak P,Kornreich R,Liao J,Lorier R,Scott SA,Smith CH,Toji LH,Turner A,Kalman LV。,遺傳變異對(duì)啟動(dòng)子使用和增強(qiáng)子活性的影響。28種藥|物遺傳基因的137種基因組DNA參考材料的表征:GeT-RM協(xié)作項(xiàng)目.18(1):109-23 2016
PubMed ID:26621101
 
Chennagiri N,White EJ,F(xiàn)rieden A,Lopez E,Lieber DS,Nikiforov A,Ross T,Batorsky R,Hansen S,Lip V,Luquette LJ,Mauceli E,Margulies D,Milos PM,Napolitano N,Nizzari MM,Yu T ,Thompson JF,Orthogonal NGS for High Throughput Clinical Diagnostics Scientific報(bào)告6:24650 2015
PubMed ID:27090146
 
Core LJ,Martins AL,Danko CG,Waters CT,Siepel A,Lis JT,新生RNA分析鑒定哺乳動(dòng)物啟動(dòng)子和增強(qiáng)子的起始區(qū)域的統(tǒng)一結(jié)構(gòu)Nature genetics46:1311-20 2014
PubMed ID:25383968
 
Zook JM,Chapman B,Wang J,Mittelman D,Hofmann O,Hide W,Salit M.,整合人類(lèi)序列數(shù)據(jù)集提供了基準(zhǔn)SNP和indel基因型調(diào)用的資源。Nat Biotechnol.32(3):246-51 2014
PubMed ID:24531798
 
Dames S,Chou LS,Xiao Y,Wayman T,Stocks J,Singleton M,Eilbeck K,Mao R,線粒體基因組的下一代測(cè)序分析和與線粒體疾|病相關(guān)的108個(gè)核基因的開(kāi)發(fā)分子診斷學(xué)期刊: JMD32(3):246-51 2013
PubMed ID:23665194
 
Carneiro MO,Russ C,Ross MG,Gabriel SB,Nusbaum C,DePristo MA,太平洋生物科學(xué)測(cè)序技術(shù),用于人類(lèi)數(shù)據(jù)中的基因分型和變異發(fā)現(xiàn)BMC基因組學(xué)13:375 2012
PubMed ID:22863213
 
Liang WS,Craig DW,Carpten J,Borad MJ,Demeure MJ,Weiss GJ,Izatt T,Sinari S,Christoforides A,Aldrich J,Kurdoglu A,Barrett M,Phillips L,Benson H,Tembe W,Braggio E,Kiefer JA ,Legendre C,Posner R,Hostetter GH,Baker A,Egan JB,Han H,Lake D,Stites EC,Ramanathan RK,F(xiàn)onseca R,Stewart AK,Von Hoff D,使用下一代測(cè)序?qū)σ认侔┗颊哌M(jìn)行全基因組鑒定PloS one7:e43192 2012
PubMed ID:23071490
 
Girirajan S,Dennis MY,Baker C,Malig M,Coe BP,Campbell CD,Mark K,Vu TH,Alkan C,Cheng Z,Biesecker LG,Bernier R,Eichler EE,改進(jìn)和發(fā)現(xiàn)新的拷貝數(shù)變異熱點(diǎn)與自閉癥譜系障礙有關(guān)的美國(guó)人類(lèi)遺傳雜志92:221-37 2012
PubMed ID:23375656
 
Peters BA1,Kermani BG,Sparks AB,Alferov O,Hong P,Alexeev A,Jiang Y,Dahl F,Tang YT,Haas J,Robasky K,Zaranek AW,Lee JH,Ball MP,Peterson JE,Perazich H,Yeung G ,Liu J,Chen L,Kennemer MI,Pothuraju K,Konvicka K,Tsoupko-Sitnikov M,Pant KP,Ebert JC,Nilsen GB,Baccash J,Halpern AL,Church GM,Drmanac R.,準(zhǔn)確的全基因組測(cè)序和單倍型分型從10到20個(gè)人體細(xì)胞。Nature487(7406):190-5 2012
PubMed ID:22785314
 
ENCODE項(xiàng)目聯(lián)盟,Dunham I,Kundaje A,Aldred SF,Collins PJ,Davis CA,Doyle F,Epstein CB,F(xiàn)rietze S,Harrow J,Kaul R,Khatun J,Lajoie BR,Landt SG,Lee BK,Pauli F,Rosenbloom KR,Sabo P,Safi A,Sanyal A,Shoresh N,Simon JM,Song L,Trinklein ND,Altshuler RC,Birney E,Brown JB,Cheng C,Djebali S,Dong X,Dunham I,Ernst J,F(xiàn)urey TS, Gerstein M,Giardine B,Greven M,Hardison RC,Harris RS,Herrero J,Hoffman MM,Iyer S,Kelllis M,Khatun J,Kheradpour P,Kundaje A,Lassman T,Li Q,Lin X,Marinov GK,Merkel A ,Mortazavi A,Parker SC,Reddy TE,Rozowsky J,Schlesinger F,Thurman RE,Wang J,Ward LD,Whitfield TW,Wilder SP,Wu W,Xi HS,Yip KY,Zhuang J,Bernstein BE,Birney E,Dunham我,Green ED,Gunter C,Snyder M,Pazin MJ,Lowdon RF,Dillon LA,Adams LB,Kelly CJ,Zhang J,Wexler JR,Green ED,Good PJ,F(xiàn)eingold EA,Bernstein BE,Birney E,Crawford GE,Dekker J,Elinitski L,F(xiàn)arnham PJ,Gerstein M,Giddings MC,Gingeras TR,Green ED,GuigóR,Hardison RC,Hubbard TJ,Kellis M,Kent WJ,Lieb JD,Margulies EH ,Myers RM,Snyder M,Starnatoyannopoulos JA,Tennebaum SA,Weng Z,White KP,Wold B,Khatun J,Yu Y,Wrobel J,Risk BA,Gunawardena HP,Kuiper HC,Maier CW,Xie L,Chen X,Giddings MC,Bernstein BE,Epstein CB,Shoresh N,Ernst J,Kheradpour P,Mikkelsen TS,Gillespie S,Goren A,Ram O,Zhang X,Wang L,Issner R,Coyne MJ,Durham T,Ku M,Truong T, Ward LD,Altshuler RC,Eaton ML,Kellis M,Djebali S,Davis CA,Merkel A,Dobin A,Lassmann T,Mortazavi A,Tanzer A,Lagarde J,Lin W,Schlesinger F,Xue C,Marinov GK,Khatun J ,Williams BA,Zaleski C,Rozowsky J,R?derM,Kokocinski F,Abdelhamid RF,Alioto T,Antoshechkin I,Baer MT,Batut P,Bell I,Bell K,Chakrabortty S,Chen X,Chrast J,Curado J,Derrien T,Drenkow J,Dumais E,Dumais J,Duttagupta R,F(xiàn)astuca M,F(xiàn)ejes-Toth K,F(xiàn)erreira P,F(xiàn)oissac S,F(xiàn)ullwood MJ,Gao H,Gonzalez D, Gordon A,Gunawardena HP,Howald C,Jha S,Johnson R,Kapranov P,King B,Kingswood C,Li G,Luo OJ,Park E,Preall JB,Presaud K,Ribeca P,Risk BA,Robyr D,Ruan X ,Sammeth M,Sandu KS,Schaeffer L,See LH,Shahab A,Skancke J,Suzuki AM,Takahashi H,Tilgner H,Trout D,Walters N,Wang H,Wrobel J,Yu Y,Hayashizaki Y,Harrow J,Gerstein M,Hubbard TJ,Reymond A,Antonarakis SE,Hannon GJ,Giddings MC,Ruan Y,Wold B,Carninci P,GuigóR,Gingeras TR,Rosenbloom KR,Sloan CA,Learned K,Malladi VS,Wong MC,Barber GP, Cline MS,Dreszer TR,Heitner SG,Karolchik D,Kent WJ,Kirkup VM,Meyer LR,Long JC,Maddren M,Raney BJ,F(xiàn)urey TS,Song L,Grasfeder LL,Giresi PG,Lee BK,Battenhouse A,Sheffield NC,Simon JM,Showers KA,Safi A,London D,Bhinge AA,Shestak C,Schaner MR,Kim SK,Zhang ZZ,Mieczkowski PA,Mieczkowska JO,Liu Z,McDaniell RM,Ni Y ,Rashid NU,Kim MJ,Adar S,Zhang Z,Wang T,Winter D,Keefe D,Birney E,Iyer VR,Lieb JD,Crawford GE,Li G,Sandhu KS,Zheng M,Wang P,Luo OJ,Shahab A,F(xiàn)ullwood MJ,Ruan X,Ruan Y,Myers RM,Pauli F,Williams BA,Gertz J,Marinov GK,Reddy TE,Vielmetter J,Partridge EC,Trout D,Varley KE,Gasper C,Bansal A,Pepke S, Jain P,Amrhein H,Bowling KM,Anaya M,Cross MK,King B,Muratet MA,Antoshechkin I,Newberry KM,McCue K,Nesmith AS,F(xiàn)isher-Aylor KI,Pusey B,DeSalvo G,Parker SL,Balasubramanian S, Davis NS,Meadows SK,Eggleston T,Gunter C,Newberry JS,Levy SE,Absher DM,Mortazavi A,Wong WH,Wold B,Blow MJ,Visel A,Pennachio LA,Elnitski L,Margulies EH,Parker SC,Petrykowska HM,Abyzov A,Aken B,Barrell D,Barson G,Berry A,Bignell A,Boychenko V,Bussotti G,Chrast J,Davidson C,Derrien T,Despacio-Reyes G,Diekhans M, Ezkurdia I,F(xiàn)rankish A,Gilbert J,Gonzalez JM,Griffiths E,Harte R,Hendrix DA,Howald C,Hunt T,Jungreis I,Kay M,Khurana E,Kokocinski F,Leng J,Lin MF,Loveland J,Lu Z ,Manthravadi D,Mariotti M,Mudge J,Mukherjee G,Notredame C,Pei B,Rodriguez JM,Saunders G,Sboner A,Searle S,Sisu C,Snow C,Steward C,Tanzer A,Tapanan E,Tress ML,van Baren MJ,Walters N,Washieti S,Wilming L,Zadissa A,Zhengdong Z,Brent M,Haussler D,Kellis M,Valencia A,Gerstein M,Raymond A,GuigóR,Harrow J,Hubbard TJ,Landt SG,F(xiàn)rietze S ,Abyzov A,Addleman N,Alexander RP,Auerbach RK,Balasubramanian S,Bettinger K,Bhardwaj N,Boyle AP,Cao AR,Cayting P,Charos A,Cheng Y,Cheng C,Eastman C,Euskirchen G,F(xiàn)leming JD,Grubert F,Habegger L,Hariharan M,Harmanci A,Iyenger S,Jin VX,Karczewski KJ,Kasowski M,Lacroute P,Lam H,Larnarre- Vincent N,Leng J,Lian J,Lindahl-Allen M,Min R,Miotto B,Monahan H,Moqtaderi Z,Mu XJ,O'Geen H,Ouyang Z,Patacsil D,Pei B,Raha D,Ramirez L,Reed B,Rozowsky J,Sboner A,Shi M,Sisu C,Slifer T,Witt H,Wu L,Xu X,Yan KK,Yang X,Yip KY,Zhang Z,Struhl K,Weissman SM,Gerstein M,F(xiàn)arnham PJ, Snyder M,Tenebaum SA,Penalva LO,Doyle F,Karmakar S,Landt SG,Bhanvadia RR,Choudhury A,Domanus M,Ma L,Moran J,Patacsil D,Slifer T,Victorsen A,Yang X,Snyder M,White KP ,Auer T,Centarin L,Eichenlaub M,Gruhl F,Heerman S,Hoeckendorf B,Inoue D,Kellner T,Kirchmaier S,Mueller C,Reinhardt R,Schertel L,Schneider S,Sinn R,Wittbrodt B,Wittbrodt J,Weng Z,Whitfield TW,Wang J,Collins PJ,Aldred SF,Trinklein ND,Partridge EC,Myers RM,Dekker J,Jain G,Lajoie BR,Sanyal A,Balasundaram G,Bates DL,Byron R,Canfield TK ,Diegel MJ,Dunn D,Ebersol AK,Ebersol AK,F(xiàn)rum T,Garg K,Gist E,Hansen RS,Boatman L,Haugen E,Humbert R,Jain G,Johnson AK,Johnson EM,Kutyavin TM,Lajoie BR,Lee K,Lotakis D,Maurano MT,Neph SJ,Neri FV,Nguyen ED,Qu H,Reynolds AP,Roach V,Rynes E,Sabo P,Sanchez ME,Sandstrom RS,Sanyal A,Shafer AO,Stergachis AB,Thomas S, Thurman RE,Vernot B,Vierstra J,Vong S,Wang H,Weaver MA,Yan Y,Zhang M,Akey JA,Bender M,Dorschner MO,Groudine M,MacCoss MJ,Navas P,Stamatoyannopoulos G,Kaul R,Dekker J ,Stamatoyannopoulos JA,Dunham I,Beal K,Brazma A,F(xiàn)licek P,Herrero J,Johnson N,Keefe D,Lukk M,Luscombe NM,Sobral D,Vaquerizas JM,Wilder SP,Batzoglou S,Sidow A,Hussami N,Kyriazopoulou-Panagiotopoulou S,Libbrecht MW,Schaub MA,Kundaje A,Hardison RC,Miller W,Giardine B,Harris RS,Wu W,Bickel PJ,Banfai B,Boley NP, Brown JB,Huang H,Li Q,Li JJ,Noble WS,Bilmes JA,Buske OJ,Hoffman MM,Sahu AO,Kharchenko PV,Park PJ,Baker D,Taylor J,Weng Z,Iyer S,Dong X,Greven M ,Lin X,Wang J,Xi HS,Zhuang J,Gerstein M,Alexander RP,Balasubramanian S,Cheng C,Harmanci A,Lochovsky L,Min R,Mu XJ,Rozowsky J,Yan KK,Yip KY,Birney EGreven M,Lin X,Wang J,Xi HS,Zhuang J,Gerstein M,Alexander RP,Balasubramanian S,Cheng C,Harmanci A,Lochovsky L,Min R,Mu XJ,Rozowsky J,Yan KK,Yip KY,Birney EGreven M,Lin X,Wang J,Xi HS,Zhuang J,Gerstein M,Alexander RP,Balasubramanian S,Cheng C,Harmanci A,Lochovsky L,Min R,Mu XJ,Rozowsky J,Yan KK,Yip KY,Birney E,人類(lèi)基因組中的DNA元素的綜合百科全書(shū)Nature489:57-74 2011
PubMed ID:22955616
 
Shen P,Wang W,Krishnakumar S,Palm C,Chi AK,Enns GM,Davis RW,Speed TP,Mindrinos MN,Scharfe C,524疾|病候選基因的高質(zhì)量DNA序列捕獲美國(guó)國(guó)家科學(xué)院院刊美利堅(jiān)合眾國(guó)108:6549-54 2011
PubMed ID:21467225
 
Dennis MY,Nuttle X,Sudmant PH,Antonacci F,Graves TA,Nefedov M,Rosenfeld JA,Sajjadian S,Malig M,Kotkiewicz H,Curry CJ,Shafer S,Shaffer LG,de Jong PJ,Wilson RK,Eichler EE,Evolution通過(guò)不完全節(jié)段重復(fù)進(jìn)行人特異性神經(jīng)SRGAP2基因的研究Cell149:912-22 2011
PubMed ID:22559943
 
Aird D,Ross MG,Chen WS,Danielsson M,F(xiàn)ennell T,Russ C,Jaffe DB,Nusbaum C,Gnirke A,分析和*小化Illumina測(cè)序文庫(kù)中的PCR擴(kuò)增偏差基因組生物學(xué)12:R18 2010
PubMed ID:21338519
 
Gnerre S,Maccallum I,Przybylski D,Ribeiro FJ,Burton JN,Walker BJ,Sharpe T,Hall G,Shea TP,Sykes S,Berlin AM,Aird D,Costello M,Daza R,Williams L,Nicol R,Gnirke A ,Nusbaum C,Lander ES,Jaffe DB,來(lái)自大規(guī)模平行序列數(shù)據(jù)的高質(zhì)量哺乳動(dòng)物基因組匯編匯編美國(guó)國(guó)家科學(xué)院院刊108:1513-8 2010
PubMed ID:21187386
 
Fisher S,Barry A,Abreu J,Minie B,Nolan J,Delorey TM,Young G,F(xiàn)ennell TJ,Allen A,Ambrogio L,Berlin AM,Blumenstiel B,Cibulskis K,F(xiàn)riedrich D,Johnson R,Juhn F,Reilly B ,Shammas R,Stalker J,Sykes SM,Thompson J,Walsh J,Zimmer A,Zwirko Z,Gabriel S,Nicol R,Nusbaum C,一種可擴(kuò)展的全自動(dòng)化過(guò)程,用于構(gòu)建序列就緒的人外顯子組靶向捕獲文庫(kù)基因組生物學(xué)12 :R1 2010
PubMed ID:21205303
 
Ewing AD,Kazazian HH,高通量測(cè)序揭示了個(gè)體人類(lèi)基因組中人類(lèi)特異性L1含量的廣泛變異基因組研究20:1262-70 2010
PubMed ID:20488934
 
McDaniell R,Lee BK,Song L,Liu Z,Boyle AP,Erdos MR,Scott LJ,Morken MA,Kucera KS,Battenhouse A,Keefe D,Collins FS,Willard HF,Lieb JD,F(xiàn)urey TS,Crawford GE,Iyer VR ,Birney E,人類(lèi)中可遺傳的個(gè)體特異性和等位基因特異性染色質(zhì)特征科學(xué)(紐約,紐約)328:235-9 2010
PubMed ID:20299549
 
Campbell CD,Sampas N,Tsalenko A,Sudmant PH,Kidd JM,Malig M,Vu TH,Vives L,Tsang P,Bruhn L,Eichler EE,分化的人類(lèi)拷貝數(shù)多態(tài)性的群體遺傳特性美國(guó)人類(lèi)遺傳學(xué)雜志88: 2010年317-32
PubMed ID:21397061
 
Stewart C,Kural D,Str?mbergMP,Walker JA,Konkel MK,StützAM,Urban AE,Grubert F,Lam HY,Lee WP,Busby M,Indap AR,Garrison E,Huff C,Xing J,Snyder MP,Jorde LB ,Batzer MA,Korbel JO,Marth GT,1000 Genomes Project GT,人體中移動(dòng)元素插入多態(tài)性的綜合圖譜PLoS genetics7:e1002236 2010
PubMed ID:21876680
 
Beck CR,Collier P,Macfarlane C,Malig M,Kidd JM,Eichler EE,Badge RM,Moran JV,人類(lèi)基因組中的LINE-1逆轉(zhuǎn)錄活性Cell141:1159-70 2010
PubMed ID:20602998
 
Ng SB,Turner EH,Robertson PD,F(xiàn)lygare SD,Bigham AW,Lee C,Shaffer T,Wong M,Bhattacharjee A,Eichler EE,Bamshad M,Nickerson DA和Shendure J. ,12個(gè)人的目標(biāo)捕獲和大規(guī)模并行測(cè)序exomes Nature461(7261):272-276 2009
PubMed ID:19684571
 
Xue Y,Zhang X,Huang N,Daly A,Gillson CJ,Macarthur DG,Yngvadottir B,Nica AC,Woodwark C,Chen Y,Conrad DF,Ayub Q,Mehdi SQ,Li P,Tyler-Smith C,Population differentiation as近期人類(lèi)正面選擇的指標(biāo):經(jīng)驗(yàn)評(píng)估Genetics183:1065-77 2009
PubMed ID:19737746
 
Park H,Kim JI,Ju YS,Gokcumen O,Mills RE,Kim S,Lee S,Suh D,Hong D,Kang HP,Yoo YJ,Shin JY,Kim HJ,Yavartanoo M,Chang YW,Ha JS,Chong W ,Hwang GR,Darvishi K,Kim H,Yang SJ,Yang KS,Kim H,Hurles ME,Scherer SW,Carter NP,Tyler-Smith C,Lee C,Seo JS,發(fā)現(xiàn)使用集成高的常見(jiàn)亞洲拷貝數(shù)變體分辨率陣列CGH和大規(guī)模并行DNA測(cè)序Nature genetics42:400-5 2009
PubMed ID:20364138
 
Antonacci F,Kidd JM,Marques-Bonet T,Ventura M,Siswara P,Jiang Z,Eichler EE,六種人類(lèi)疾|病相關(guān)反轉(zhuǎn)多態(tài)性的表征人類(lèi)分子遺傳學(xué)42:400-5 2009
PubMed ID:19383631
 
Riethman H,人類(lèi)亞端??截悢?shù)變異細(xì)胞遺傳學(xué)和基因組研究123:244-52 2008
PubMed ID:19287161
 
Podder M,Ruan J,Tripp W,Chu E,Tebbutt J,Robust SNP基因分型通過(guò)多重PCR和陣列引物延伸BMC醫(yī)學(xué)基因組學(xué)1:5 2007
PubMed ID:18237385
 
Kidd JM,Cooper GM,Donahue WF,Hayden HS,Sampas N,Graves T,Hansen N,Teague B,Alkan C,Antonacci F,Haugen E,Zerr T,Yamada NA,Tsang P,Newman TL,TüzünE,Cheng Z ,Ebling HM,Tusneem N,David R,Gillett W,Phelps KA,Weaver M,Saranga D,Brand A,Tao W,Gustafson E,McKernan K,Chen L,Malig M,Smith JD,Korn JM,McCarroll SA,Altshuler DA,Peiffer DA,Dorschner M,Stamatoyannopoulos J,Schwartz D,Nickerson DA,Mullikin JC,Wilson RK,Bruhn L,Olson MV,Kaul R,Smith DR,Eichler EE,來(lái)自八個(gè)人類(lèi)基因組的結(jié)構(gòu)變異的定位和測(cè)序Nature453: 2007年56-64
PubMed ID:18451855
 
Bovee D,Zhou Y,Haugen E,Wu Z,Hayden HS,Gillett W,Tuzun E,Cooper GM,Sampas N,Phelps K,Levy R,Morrison VA,Sprague J,Jewett D,Buckley D,Subramaniam S,Chang J ,Smith DR,Olson MV,Eichler EE,Kaul R,利用多個(gè)人產(chǎn)生的fosmid資源填補(bǔ)人類(lèi)基因組中的空白Nature genetics40:96-101 2007
PubMed ID:18157130
 
de Bakker PI,McVean G,Sabeti PC,Miretti MM,Green T,Marchini J,Ke X,Monsuur AJ,Whittaker P,Delgado M,Morrison J,Richardson A,Walsh EC,Gao X,Galver L,Hart J,Hafler DA,Pericak-Vance M,Todd JA,Daly MJ,Trowsdale J,Wijmenga C,Vyse TJ,Beck S,Murray SS,Carrington M,Gregory S,Deloukas P,Rioux JD,高分辨率HLA和SNP單倍型圖譜擴(kuò)展的人MHC Nature Genetics38(10):1166-1172 2006中的疾|病關(guān)聯(lián)研究
PubMed ID:16998491
 
Redon R,Ishikawa S,F(xiàn)itch KR,F(xiàn)euk L,Perry GH,Andrews TD,F(xiàn)iegler H,Shapero MH,Carson AR,Chen W,Cho EK,Dallaire S,F(xiàn)reeman JL,GonzálezJR,GratacòsM,Huang J,Kalaitzopoulos D ,Komura D,MacDonald JR,Marshall CR,Mei R,Montgomery L,Nishimura K,Okamura K,Shen F,Somerville MJ,Tchinda J,Valsesia A,Woodwark C,Yang F,Zhang J,Zerjal T,Zhang J,Armengol L,Conrad DF,Estivill X,Tyler-Smith C,Carter NP,Aburatani H,Lee C,Jones KW,Scherer SW,Hurles ME,人類(lèi)基因組中拷貝數(shù)的全球變異Nature444:444-54 2006
PubMed ID:17122850
 
Miretti MM,Walsh EC,Ke X,Delgado M,Griffiths M,Hunt S,Morrison J,Whittaker P,Lander ES,Cardon LR,Bentley DR,Rioux JD,Beck S,Deloukas P,高分辨率連鎖不平衡圖人類(lèi)主要組織相容性復(fù)合物和第|一代標(biāo)簽單核苷酸多態(tài)性。Am J Hum Genet76(4):634-46 2005
PubMed ID:15747258
 
Altshuler D,Brooks LD,Chakravarti A,Collins FS,Daly MJ,Donnelly P; 國(guó)際HapMap聯(lián)盟,人類(lèi)基因組的單倍型圖譜。Nature437(7063):1299-320 2005
PubMed ID:16255080
 
Altshuler D,Brooks LD,Chakravarti A,Collins FS,Daly MJ,Donnelly P; 國(guó)際HapMap聯(lián)盟,人類(lèi)基因組的單倍型圖譜。Nature437(7063):1299-320 2005
PubMed ID:16255080
 
Matsuzaki H,Dong S,Loi H,Di X,Liu G,Hubbell E,Law J,Berntsen T,Chadha M,Hui H,Yang G,Kennedy GC,Webster TA,Cawley S,Walsh PS,Jones KW,F(xiàn)odor SP ,Mei R,在一對(duì)寡核苷酸陣列上對(duì)超過(guò)100,000個(gè)SNP進(jìn)行基因分型。Nat Methods1(2):109-11 2004
PubMed ID:15782172

滬公網(wǎng)安備 31011002002624號(hào)