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Imikhiqizo

Ukuhlaziywa kwe-Bulked Secregant

Ukuhlaziywa kwe-Bulked Secregant (BSA) inqubo esetshenzisiwe ukukhomba amamaki wofuzo ahlobene nohlobo lwe-phenotype. Ukuhamba komsebenzi okuyinhloko kwe-BSA kuqukethe ukukhetha amaqembu amabili abantu abanama-phenotypes aphikisanayo, bafaka i-DNA yabo bonke abantu ukuze basebenzise inqwaba ye-DNA, ikhomba ukulandelana kwamachibi amabili phakathi kwamachibi amabili. Le ndlela isetshenziswe kabanzi ekuboneni amamaki ofuzo ahlotshaniswa ngokuqinile ngohlobo olubhekiswe kuzakhi zofuzo ezihlosiwe ku-plant / animal genomes.


Imininingwane ye-Service

Imiphumela yedemo

Ucwaningo lwesigameko

Izinzuzo zensizakalo

Okuqophele

Tatagi et al., Iphephabhuku lezitshalo, 2013

● Ukuhlelwa kwendawo okunembile: ukuxuba ama-bulks nabangu-30 kuya ku-200 abantu abangu-200 ukuze banciphise umsindo wangemuva; ukubikezela okungafani nokufundwayo okusekelwe endabeni.

● Ukuhlaziywa okuphelele: Isichasiselo se-gene yofuzo elijulile, kufaka phakathi i-NR, SwissProt, Go, Kegg, COG, KOG, njll.

● Isikhathi esiguqukayo ngokushesha: I-Rapid gene yasendaweni ukuzokwenza ngaphakathi kwezinsuku ezingama-45 zomsebenzi.

● Umuzwa obanzi: I-BMK iba negalelo ezinkulungwaneni zezici zasendaweni, emboza izinhlobo ezahlukahlukene njengezitshalo, imikhiqizo yasemanzini, ihlathi, izimbali, izithelo, njll.

Ukucaciswa Kwensiza

Inani labantu:
Ukuhlukaniswa inzalo yabazali abane-phenotypes ephikisayo.
I-EG F2 Progeny, i-Backcrossing (BC), I-Recombivent InBred Line (RIL)

Ukuxuba Ichibi
Ngezimpawu ezifanelekile: abantu abangama-30 kuye kwangama-50 (ubuncane be-20) / inqwaba
Nge-Tratis yenani: I-5% ephezulu kuya ku-10% abantu abane-phenotypes ebabazekayo kubo bonke abantu (ubuncane 30 + 30).

Ukujula okuncomekayo kokulandelana
Okungenani i-20x / umzali no-1x / inzalo / inzalo echibini lokuxuba inzalo elingu-30 + 30 umuntu ngamunye, ukujula okubuyiselwe kuzoba ngu-30x ngobuningi ngakunye)

Ama-Bioinformatics ahlaziya

● Ukuvuselela okuphelele kofuzo
 
● Ukucutshungulwa kwedatha
 
● I-SNP / Indel Calling
 
● Ukuhlolwa kwesifunda esifundeni
 
● Isichasiselo se-gene yofuzo

流程图 -BS-A1

Izidingo zesampula nokulethwa

Izidingo zesampula:

I-nucleotides:

isampula le-gdna

Isampula yezicubu

Ukuhlushwa: ≥30 ng / μl

Izitshalo: 1-2 g

Inani: ≥2 μg (Volummun ≥15 μl)

Izilwane: 0.5-1 g

Ukumsulwa: OD260 / 280 = 1.6-2.5

Igazi eliphelele: 1.5 ml

Ukugeleza komsebenzi wesevisi

Isampula Qc

Idizayini yokuhlola

ukulethwa kwesampula

Ukulethwa kwesampula

Ukuhlolwa kwe-Pilot

Ukukhishwa kwe-RNA

Ukulungiselela umtapo

Ukwakhiwa Kwelabhulali

Ukulandelana

Ukulandelana

Ukuhlaziywa kwedatha

Ukuhlaziywa kwedatha

Ngemuva Kwezinsizakalo Zokuthengisa

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  • Okwedlule:
  • Olandelayo:

  • Isisekelo sokuhlaziywa kwe-1.Association ebangeni lase-Euclidean Kulesi sibalo esilandelayo

    I-X-axis: Inombolo ye-Chromosome; I-dot ngayinye imele inani le-snp. Umugqa omnyama uhambelana nenani elifanelekile. Inani eliphakeme eliphakeme libonisa ubudlelwane obukhulu phakathi kwesiza kanye ne-phenotype. Umugqa we-Red Dash umele umkhawulo wenhlangano ebalulekile.

    I-MRNA-FLNC-Read-Hered-Distribution

     

    Ukuhlaziywa kwe-2.Association kusekelwe akukho nkomba ye-SNP-Index

    I-X-axis: Inombolo ye-Chromosome; I-DOT ngayinye imele inani lenkomba ye-SNP. Umugqa omnyama ume ngenani le-SNP-Index. Okukhulu inani, kubaluleke kakhulu inhlangano.

    I-MRNA-RNA-ORF-HLE ESISUKU

     

    Icala leBMK

    I-Locus ye-Local-Efficial Fetital Fnl7.1 I-Flote WNSROGEGENEIS IPROTEIN enkulu ehlotshaniswa nobude bentamo yezithelo ekhukhamba

    Ishicilelwe: I-FRIT BIOTECHnology Journal, 2020

    Isu lokulandelana:

    Bazali (Jin5-508, yn): Yonke indawo yokuphumula yofuzo i-34 × no 20 ×.

    Amachibi e-DNA (ama-50 akhulelwe ama-50 futhi angama-50 amafushane): Ukubuyiselwa kabusha kwe-61 × no-52 ×

    Imiphumela Esemqoka

    Kulolu cwaningo, ukwahlukanisa inani labantu (F2 ne-F2: 3) kwenziwa ngokuwela umugqa wekhukhamba omude JIN5-508 kanye nentamo ye-yn emfushane. Amachibi amabili e-DNA akhiwa ngabantu abangu-50 abade bentamo ende nabangu-50 abantu abanentamo abafushane. I-QTL enkulu ye-QTL ikhonjwe ku-CHR07 ngokuhlaziywa kwe-BSA kanye nemephu yendabuko yendabuko. Isifunda sokhetho saphinde sancishiswa phansi ngemephu enhle, ukucaciswa kwezichasiso zofuzo kanye nokuhlolwa kwe-transgenic, okuveze uhlobo olusemqoka ekulawuleni ubude bentambo, i-CSFNL7.1. Ngaphezu kwalokho, i-polymorphism ku-CSFNL7.1 Region Region Region yatholakala ihlobene nenkulumo ehambisanayo. Ukuhlaziywa okwengeziwe kwe-phylogenetic kuphakanyiswe ukuthi i-FNL7.1 I-Locus kungenzeka ukuthi yasungulwa e-India.

    I-PB-FET-FET-RNA-SEQUECING-Study-Study

    Imephu ye-QTL ekuhlaziyweni kwe-BSA ukukhomba isifunda sokhetho oluhlotshaniswa nobude bemomo yekhukhamba

    I-PB-FET-FET-RNA-RNA-SPOSSIP

    Amaphrofayili weLod amakhukhamba ubude qtl akhonjwe ku-CH07

     
    Inkomba

    UXu, X., et al. "I-Locus ye-Locutital ye-Majour-Found Locus FNL7.1.1 Ifaka amaprotheni amaningi we-mburry anlogenes ahlotshaniswa nobude bentamo yezithelo ekhukhamba." Plant biotechnology Journal 18.7 (2020).

    Thola isilinganiso

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