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Imikhiqizo

Isitshalo / isilwane sonke se-genome

Ukulandelana okuphelele kofuzo (WGS), owaziwa nangokuthi ukubuyiselwa emuva, kubhekisele ekuhlolweni kolunye uhlobo lwabantu abahlukahlukene ezinhlotsheni ezahlukahlukene ngolwazi olwaziwayo lwe-genomes. Ngalesi sisekelo, umehluko we-genomic wabantu noma abantu ungaphinde ukhonjwe. I-WGS inika amandla ukukhonjwa kwe-nucleotide ye-nucleotide polymorphism (SNP), ukusulwa kokufaka (i-Indel), ukuhlukahluka kwesakhiwo (i-SV), bese ukopisha ukuhlukahluka kwenombolo (CNV). I-SVS ihlanganisa ingxenye enkulu yesisekelo sokuhluka kune-SNPS futhi ibe nomthelela omkhulu e-Genome, ethinta kakhulu izinto eziphilayo. Ngenkathi ukubuyiselwa kokufunda okufushane kuyaphumelela ekuboneni i-SNPS nama-Indels, ukubuyiselwa kwemali okude kuvumela ukukhonjwa okuqondile kwezingcezwana ezinkulu kanye nokwahlukahlukana okuyinkimbinkimbi.


Imininingwane ye-Service

Bioinformatics

Umphumela wedemo

Izincwadi Ezifakiwe

Izici Zensizakalo

● Ukulungiselela umtapo wezincwadi kungaba ngcono noma nge-PCR-free

● Kutholakala kumapulatifomu wokulandelana 4 wokulandelana: I-Illina NovaseQ, MGI T7, i-Nanopore Promethotion P48, noma i-Pacbio Revuo.

● Ukuhlaziywa kwe-bioinformatic kugxile ekutholeni okuhlukahlukene: I-SNP, Indel, SV ne-CNV

Izinzuzo zensizakalo

Ubuchwepheshe obubanzi namarekhodi okushicilela: Okuhlangenwe nakho okuqoqiwe ekulandeleni kwe-genome kwezinhlobo ezingaphezu kuka-1000 kuholele emacaleni angaphezu kwe-1000 ashicilelwe ngesici sethonya elibandayo labantu abangaphezu kuka-5000.

Ukuhlaziywa okuphelele kwe-bioinformatics: Kubandakanya ukuguquguquka kokushintshana kanye nesichasiso somsebenzi.

● Ukwesekwa kwangemva kokuthengisa:Ukuzibophezela kwethu kunwebeka ngaphezu kokuphothulwa kwephrojekthi ngesikhashana sezinyanga ezi-3 ngemuva kokuthengisa. Ngalesi sikhathi, sinikezela ngokulandela iphrojekthi, usizo lokuxazulula inkinga, kanye ne-q & amaseshini ukubhekana nanoma yimiphi imibuzo ehlobene nemiphumela.

Isichasiso esibanzi: Sisebenzisa ama-databases amaningi ukuze akwazisa ngokusebenza kwezakhi zofuzo ngokuhlukahluka okuhlonziwe futhi enze ukuhlaziya okuhambisanayo kokucebisa, ukuhlinzeka ngemininingwane kumaphrojekthi wokucwaninga amaningi.

Ukucaciswa Kwensiza

Ukuhlukahluka okuzokhonjwa

Ukuhlehlisa Isu

Ukujula okunconyiwe

I-SNP ne-Indel

I-Illumina Novaseq PE150

noma i-MGI T7

Eliyo

I-SV ne-CNV (inembile kangako)

I-30x

I-SV ne-CNV (kunembe kakhudlwana)

I-Nanopore Prom P48

20x

I-SNPS, Indels, SV ne-CNV

I-Pacbio Revuo

Eliyo

Izidingo zesampula

Izicubu noma ama-nucleic acid ama-nucleic

I-Illumina / MGI

I-nanopore

Pacbio

 

Isilwane se-viscera

0.5-1 g

≥ 3.5 g

 

≥ 3.5 g

 

Izicubu zezilwane

≥ 5 g

 

≥ 5 g

 

Igazi LaseMammalian

1.5 ml

≥ 0.5 ml

 

≥ 5 ml

 

I-PoulTry / Igazi Lezinhlanzi

≥ 0.1 ml

 

≥ 0.5 ml

 

Isitshalo- iqabunga elisha

1-2 g

≥ 2 g

 

≥ 5 g

 

Amaseli abunjiwe

 

≥ 1x107

 

≥ 1x108

 

Izicubu ezithambile zezinambuzane / umuntu ngamunye

0.5-1 g

≥ 1 g

 

≥ 3 g

 

Kukhishwe i-DNA

 

Ukugxila: ≥ 1 ngl

Inani: ≥ 30 ng

Kukhawulelwe noma akukho ukucekelwa phansi noma ukungcoliswa

 

Ukuqoqana

Inani

 

I-OD260 / 280

 

I-OD260 / 230

 

Kukhawulelwe noma akukho ukucekelwa phansi noma ukungcoliswa

 

≥ ≥ ng / μl

4 μg / ukugeleza iselula / isampula

 

1.7-2.2

 

≥1.5

Ukuqoqana

Inani

 

I-OD260 / 280

 

I-OD260 / 230

 

Kukhawulelwe noma akukho ukucekelwa phansi noma ukungcoliswa

≥ ≥ ng / μl

I-10 μg / i-Flow Cell / Isampula

 

1.7-2.2

 

1.8-2.5

Ukulungiselela umtapo wamahhala kwe-PCR-Free:

Okuhlaziyelayo 40 ng / μl

Inani 500 ng

Ukugeleza komsebenzi wesevisi

ukulethwa kwesampula

Ukulethwa kwesampula

Ukuhlolwa kwe-Pilot

Ukukhishwa kwe-DNA

Ukulungiselela umtapo

Ukwakhiwa Kwelabhulali

Ukulandelana

Ukulandelana

Ukuhlaziywa kwedatha

Ukuhlaziywa kwedatha

数据上传 -03

Ukulethwa Kwedatha


  • Okwedlule:
  • Olandelayo:

  • 流程图 7-02

    Kubandakanya ukuhlaziywa okulandelayo:

    • Ukulawulwa kwekhwalithi yedatha eluhlaza
    • Izibalo zokuqondanisa ukuze zibhekwe i-genome genome
    • Ukuhlonza okuhlukile: I-SNP, Indel, SV ne-CNV
    • Isichasiselo esisebenzayo sokuhlukahluka

    Izibalo zokuqondanisa ukuze zibhekwe i-genome yereferensi - Ukulandelana kokusatshalaliswa kokujula

     

    图片 26

     

    I-SNP ibiza phakathi kwamasampula amaningi

     

    图片 27

     

    Ukukhonjwa kwe-Indel - Izibalo zobude be-Indel esifundeni se-CDS kanye nesifunda sase-Genome-Wide

     

    图片 28

     

    Ukusatshalaliswa okuhlukile kulo lonke uhlobo lwe-genome - uzungu lwe-circos

    图片 29

    Isichasiso esisebenzayo sezakhi zofuzo ngokuhlukahluka okuhlonziwe - i-gene ontology

     

    图片 30

    I-Chai, Q. et al. . 433. Doi: 10.11111 / PBI.13965.

    UCheng, H. et al. (2023) 'I-Chromosome-Level Wild Hevea Brasiliensis Geneasiensis Genes inikeza amathuluzi amasha okuzala afungelwe kwezolona kanye ne-lociate ebalulekile ukukhulisa isivuno senjoloba', isitshalo se-biotechnology Journal, 21 (5), PP. 1058-1072. DOI: 10.11111 / PBI.14018.

    Li, a. et al. . DOI: 10.1038 / S42003-021-02823-6.

    Zeng, T. et al. (2022) Ukuhlaziywa kwe-genome ne-methylation inkukhuna yendabuko yaseChinese ngokuhamba kwesikhathi kuhlinzeka ngokuqonda ngezinhlobo zezilwane ezilondoloziwe ', i-5 (1), i-PP. 1-12. Doi: 10.1038 / S42003-022-03907-7.

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