{"title":"SECUENCIACIÓN COMPLETA DEL GENOMA (WGS)","description":"","products":[{"product_id":"genoma-mitocondrial-adn-mitocondrial","title":"Mitochondrial genome Mitochondrial DNA","description":"","brand":"Cidegen","offers":[{"title":"Default Title","offer_id":51600374071562,"sku":"1309","price":1633.5,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0900\/6661\/6586\/files\/propuestas_cambio_diseno_genotica_11.png?v=1758022922"},{"product_id":"genoma-completo-wgs-duo","title":"Whole Genome WGS Duo","description":"\u003cp\u003e cWGS: NGS + CNV + mtDNA + UPD + repeat expansions + medical report for index and 2 family members.\u003cbr\u003e\n Raw and processed data available for download free of charge for a period of 30 days via CentoPortal.\u003c\/p\u003e","brand":"Pronacera Therapeutics","offers":[{"title":"Default Title","offer_id":51600382394634,"sku":"1253","price":3920.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0900\/6661\/6586\/files\/propuestas_cambio_diseno_genotica_11.png?v=1758022922"},{"product_id":"genoma-completo-wgs","title":"Whole genome WGS","description":"\u003cp\u003e cWGS: NGS + CNV + mtDNA + UPD + repeat expansions + medical report for index and 1 family member.\u003cbr\u003e\n Raw and processed data available for download free of charge for a period of 30 days via CentoPortal.\u003c\/p\u003e","brand":"Pronacera Therapeutics","offers":[{"title":"Default Title","offer_id":51600382460170,"sku":"1252","price":1960.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0900\/6661\/6586\/files\/propuestas_cambio_diseno_genotica_11.png?v=1758022922"},{"product_id":"allaboutme-exoma-medicina-personalizada","title":"AllAboutMe - exome - personalized medicine","description":"\u003cp\u003eKnowing your DNA sequence helps us understand how your body works and allows us to recommend lifestyle changes or provide follow-up or treatment tailored to your case. Only with genetic information can we apply the 5Ps of medicine: predictive, preventative, personalized, precision, and participatory. The test is based on the complete sequencing of a person's exome, that is, of the more than 20,000 genes in the genome. This technology allows us to customize the study according to your personal and family history. The test includes a genetic counseling consultation before and after the test. The report contains information about:\u003cbr\u003e\n + 125 genes responsible for actionable diseases*\u003cbr\u003e\n + 50 important genes in the prevention of hereditary cancer\u003cbr\u003e\n + 150 genes important in reproduction (carrier and fertility)\u003cbr\u003e\n + 180 drugs involved in pharmacogenetic responses\u003cbr\u003e\n + 30 genes involved in response to food and nutrition\u003cbr\u003e \n+ 20 characteristics associated with well-being and lifestyle\u003cbr\u003e\n + 30 subpopulations and ancestral characteristics in an origins report\u003cbr\u003e\n + personalized gene panel based on your personal and family history\"\u003c\/p\u003e","brand":"ADNinstitut","offers":[{"title":"Default Title","offer_id":51600421716234,"sku":"1035","price":545.0,"currency_code":"EUR","in_stock":false}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0900\/6661\/6586\/files\/propuestas_cambio_diseno_genotica_5.png?v=1767115739"},{"product_id":"aboutme-ancestros","title":"AboutMe - Ancestors","description":"\u003cp\u003e \"The analysis involves reconstructing your genetic ancestry by comparing your genetic makeup with a defined population group. Your genetic data, obtained from the analysis of over 850,000 variants, allows us to gain insight into:\u003cbr\u003e\n - Your origins based on comparison with 2,500 genomes from 26 distinct populations\u003cbr\u003e\n - Paternal origin (Y chromosome haplogroup) and maternal origin (mitochondrial DNA haplotype) in men and maternal origin in women\u003cbr\u003e\n - Percentage of admixture with Homo neanderthalensis.\u003cbr\u003e\n - \"Index of consanguinity\"\u003c\/p\u003e","brand":"ADNinstitut","offers":[{"title":"Default Title","offer_id":51600421749002,"sku":"1034","price":149.0,"currency_code":"EUR","in_stock":false}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0900\/6661\/6586\/files\/propuestas_cambio_diseno_genotica_3.png?v=1757950030"},{"product_id":"aboutme-farmacogenetica","title":"AboutMe - Pharmacogenetics","description":"\u003cp\u003e Pharmacogenetics is a field of study that evaluates the effect of genetic variants on the response to certain medications. 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The test includes the analysis of 17 genes involved in more than 60 medications.\u003c\/p\u003e","brand":"ADNinstitut","offers":[{"title":"Default Title","offer_id":51600422011146,"sku":"1033","price":199.0,"currency_code":"EUR","in_stock":false}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0900\/6661\/6586\/files\/propuestas_cambio_diseno_genotica_11.png?v=1758022922"},{"product_id":"secuenciacion-de-genoma-mitocondrial","title":"Mitochondrial Genome Sequencing","description":"\u003cp\u003e Mass sequencing technology is most cost-effective when several similar diseases with different related genes are suspected.\u003cbr\u003e\n Technique: Next-generation sequencing (NGS). 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Medications can cause adverse reactions, resulting in significant morbidity, therapeutic failure, and even mortality, as well as increased healthcare costs.\u003c\/p\u003e","brand":"GenoLife","offers":[{"title":"Muestra extraída en un centro colaborador autorizado [Coste Adicional - Según zona] \/ Hisopo Bucal \/ Saliva","offer_id":52591906029834,"sku":"GENL-0049-02-1","price":309.6,"currency_code":"EUR","in_stock":true},{"title":"Muestra extraída en un centro colaborador autorizado [Coste Adicional - Según zona] \/ Sangre EDTA","offer_id":52591906062602,"sku":"GENL-0049-02-2","price":309.6,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0900\/6661\/6586\/files\/propuestas_cambio_diseno_genotica_11.png?v=1758022922"},{"product_id":"cariotipo-molecular-array-cgh-de-restos-fetales-perdida-de-embarazo","title":"Molecular karyotyping (Array CGH) of fetal remains (pregnancy loss)","description":"\u003cp\u003e This analysis can identify numerical chromosomal abnormalities, structural imbalances\u003cbr\u003e\n Genome-wide rearrangements and copy number changes, covering regions of known clinical importance (recognized microduplication\/microdeletion)\u003cbr\u003e\n syndromes), pericentromeric and subtelomeric regions, and the genomic backbone. It uses a custom-designed Illumina single nucleotide polymorphism (SNP) array. This array contains more than 630,000 SNP markers spanning both coding and non-coding sequences of the human genome. The average spatial resolution between probes is 4.5 kb.\u003c\/p\u003e","brand":"GenoLife","offers":[{"title":"Default Title","offer_id":51600447996170,"sku":"913","price":796.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0900\/6661\/6586\/files\/propuestas_cambio_diseno_genotica_11.png?v=1758022922"},{"product_id":"cariotipo-molecular-400k","title":"Molecular Karyotype 400K","description":"\u003cp\u003e Array CGH for the diagnosis of neuropediatric patients in cases requiring high-resolution studies.\u003cbr\u003e\n It analyzes the entire genome with an average detection capacity of 25 Kb, more than 100 times the resolution of conventional karyotyping.\u003c\/p\u003e","brand":"GenoLife","offers":[{"title":"Default Title","offer_id":51600448127242,"sku":"910","price":1326.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0900\/6661\/6586\/files\/propuestas_cambio_diseno_genotica_11.png?v=1758022922"},{"product_id":"cariotipo-molecular-180k","title":"Molecular Karyotype 180K","description":"\u003cp\u003e Array CGH aimed at the study of neurodevelopmental disorders and polymalformative syndromes.\u003cbr\u003e \nIt analyzes 308 OMIM syndromes, along with other genetic regions responsible for various pathologies. It offers a minimum resolution of 75 kb in the syndromic regions and 40 kb in the critical genes. The rest of the genome is analyzed with an average resolution of 350 kb.\u003c\/p\u003e","brand":"GenoLife","offers":[{"title":"Default Title","offer_id":51600448192778,"sku":"908","price":911.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0900\/6661\/6586\/files\/propuestas_cambio_diseno_genotica_11.png?v=1758022922"},{"product_id":"cariotipo-molecular-60k","title":"Molecular Karyotype 60K","description":"\u003cp\u003e Array CGH aimed at the study of polymalformative syndromes, with or without intellectual disability.\u003cbr\u003e\n It analyzes 308 OMIM syndromes, along with other genetic regions responsible for various pathologies. It offers a minimum resolution of 100 kb in the syndromic regions and 50 kb in the critical genes. The rest of the genome is analyzed with an average resolution of 350 kb.\u003c\/p\u003e","brand":"GenoLife","offers":[{"title":"Default Title","offer_id":51600449372426,"sku":"907","price":911.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0900\/6661\/6586\/files\/propuestas_cambio_diseno_genotica_11.png?v=1758022922"},{"product_id":"secuenciacion-de-exoma-completo-dirigido-mas-genoma-mitocondrial","title":"Whole Exome Sequencing, Targeted plus Mitochondrial Genome","description":"\u003cp\u003eMass sequencing technology is most cost-effective when several similar diseases with different related genes are suspected.\u003cbr\u003e\n Technique: Next-generation sequencing (NGS). The Novaseq 6000® system is used with the SureSelect V6 sequencing panel, and Nextera XT (NGS) is used for the mitochondrial genome.\u003c\/p\u003e","brand":"GenoLife","offers":[{"title":"Default Title","offer_id":51600452452618,"sku":"886","price":1704.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0900\/6661\/6586\/files\/propuestas_cambio_diseno_genotica_11.png?v=1758022922"},{"product_id":"genexvitae","title":"GeneXvitae","description":"\u003cp\u003e A comprehensive, simple, and accurate genetic test that allows us to establish a personalized nutritional action plan.\u003c\/p\u003e\n\n\n\u003cp\u003e With an innovative approach to personalized medicine, it provides:\u003c\/p\u003e\n\n\n\u003cp\u003e 1. Global and integrated vision of the genetic profile of each individual.\u003cbr\u003e\n 2. Practical and simple genetic information that impacts the patient's daily life and quality of life.\u003cbr\u003e\n 3. A detailed action plan designed based on each patient's individual genomic information. These recommendations are useful for avoiding unnecessary nutritional restrictions and allow for the development of a nutritional plan tailored to each individual's metabolism, thus facilitating the achievement of long-term goals.\u003c\/p\u003e","brand":"Pronacera Therapeutics","offers":[{"title":"Default Title","offer_id":51600559440138,"sku":"24","price":300.0,"currency_code":"EUR","in_stock":true}]},{"product_id":"secuenciacion-genoma-completo-30x-90-gb-sample-raw-data","title":"Whole genome sequencing (30x 90 Gb\/sample) - raw data","description":"\u003cp\u003e Delivery of raw data from the requested sequencing study.\u003c\/p\u003e","brand":"ADNInstitut","offers":[{"title":"Default Title","offer_id":52502727459082,"sku":"ADNI-0123-10-1","price":985.0,"currency_code":"EUR","in_stock":true}]},{"product_id":"secuenciacion-de-genoma-completo","title":"Whole Genome Sequencing","description":"\u003cp\u003e Whole genome sequencing by NGS\u003c\/p\u003e","brand":"GenoLife","offers":[{"title":"1. Muestra extraída directamente en la clínica o centro solicitante [+0,00€] \/ Hisopo Bucal \/ Saliva","offer_id":52574469751050,"sku":"GENL-0008-07-1","price":1260.0,"currency_code":"EUR","in_stock":true},{"title":"1. Muestra extraída directamente en la clínica o centro solicitante [+0,00€] \/ Sangre EDTA","offer_id":52574469783818,"sku":"GENL-0008-07-2","price":1260.0,"currency_code":"EUR","in_stock":true}]},{"product_id":"adntro-secuenciacion-completa-del-genoma-wgs","title":"SECUENCIACIÓN COMPLETA DEL GENOMA (WGS 30x) - ADNTRO","description":"\u003ch3\u003e\n\u003cstrong\u003eDESCRIPCIÓN\u003c\/strong\u003e\u003cstrong\u003e\u003c\/strong\u003e\n\u003c\/h3\u003e\n\u003ch4\u003e\u003cstrong\u003e¿TIENES SOSPECHA DE ALGUNA PATOLOGÍA GENÉTICA? \u003c\/strong\u003e\u003c\/h4\u003e\n\u003cdiv\u003eEn ese caso, la tecnología más adecuada es la \u003cspan class=\"s1\"\u003e\u003cb\u003esecuenciación completa del genoma (Whole Genome Sequencing, WGS)\u003c\/b\u003e\u003c\/span\u003e, que permite analizar la totalidad del ADN y detectar variantes genéticas relevantes con el máximo nivel de profundidad y precisión.\u003c\/div\u003e\n\u003cdiv\u003e\u003cbr\u003e\u003c\/div\u003e\n\u003cdiv\u003eAnalizamos todo tu ADN. Toda la información. Descubre qué variantes esconde tu ADN y toma medidas basadas en tu información genética. Analizamos \u003cem\u003ehasta 3.000 millones de marcadores (el 100 % de tu ADN)\u003c\/em\u003e con los más altos estándares de calidad y garantizando tu privacidad. Elige la prueba genética más completa y precisa disponible.\u003c\/div\u003e\n\u003cdiv\u003e\u003cbr\u003e\u003c\/div\u003e\n\u003cdiv\u003e\n\u003cb\u003e\u003c\/b\u003e\u003cbr\u003e\n\u003c\/div\u003e\n\u003ch3\u003e\u003cb\u003eQUÉ INCLUYE EL TEST\u003c\/b\u003e\u003c\/h3\u003e\n\u003cp\u003e\u003cspan\u003e\u003cmeta charset=\"utf-8\"\u003e• \u003cstrong\u003eSecuenciación\u003c\/strong\u003e completa del \u003cstrong\u003egenoma\u003c\/strong\u003e: análisis de todos los SNPs de tu ADN, tanto comunes como poco frecuentes.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003cstrong\u003e\u003cmeta charset=\"utf-8\"\u003e• Validez\u003c\/strong\u003e para \u003cstrong\u003ediagnóstico\u003c\/strong\u003e clínico.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e • \u003cstrong\u003eAlta cobertura y precisión\u003c\/strong\u003e analítica.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e • \u003cstrong\u003eInforme detallado\u003c\/strong\u003e con parámetros de calidad.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e • \u003cstrong\u003eFarmacogenética clínica\u003c\/strong\u003e: posible ajuste de dosis de fármacos con validez clínica.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e • \u003cstrong\u003eEstado de portador\u003c\/strong\u003e: identificación de enfermedades genéticas que podrían heredarse a la descendencia.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e • \u003cem\u003eAcceso al informe ADNTRO\u003c\/em\u003e: análisis de una amplia variedad de rasgos comunes y predisposiciones genéticas. --\u0026gt; Ver \u003cspan style=\"color: rgb(255, 128, 0);\"\u003e\u003cstrong\u003e\u003ca href=\"https:\/\/adntro.com\/wp-content\/uploads\/2025\/09\/ADNTRO-Informe-ejemplo-reporte.pdf\" style=\"color: rgb(255, 128, 0);\" rel=\"noopener\" target=\"_blank\"\u003einforme de ejemplo\u003c\/a\u003e\u003c\/strong\u003e\u003c\/span\u003e.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e • \u003cem\u003eActualizaciones periódicas\u003c\/em\u003e: incorporación continua de nuevos informes y hallazgos científicos.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e • \u003cstrong\u003eActivos genéticos\u003c\/strong\u003e: además de la interpretación de resultados, te entregamos tus archivos genéticos en bruto.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003eUn \u003cstrong\u003etest integral para descifrar todo lo que esconde tu ADN, sin salir de casa\u003c\/strong\u003e. Recibirás el kit para recolectar tu muestra de ADN en el domicilio. \u003c\/p\u003e\n\u003cdiv\u003eAdemás, durante todo el proceso contarás con el apoyo de nuestro equipo médico (*), que te asesorará, te explicará los informes en detalle y te ayudará a tomar medidas preventivas personalizadas para cuidar al máximo de tu salud.\u003c\/div\u003e\n\u003cdiv\u003e\u003cbr\u003e\u003c\/div\u003e\n\u003cdiv style=\"text-align: left;\"\u003e\u003cimg src=\"https:\/\/cdn.shopify.com\/s\/files\/1\/0900\/6661\/6586\/files\/caja_Kit_adntro.png?v=1765844807\" alt=\"\" width=\"350\" height=\"274\" style=\"display: block; margin-left: auto; margin-right: auto;\"\u003e\u003c\/div\u003e\n\u003cdiv\u003e\n\u003cmeta charset=\"utf-8\"\u003e\n\u003ch3\u003e\u003cstrong\u003eENVÍO Y RECEPCIÓN DE LA MUESTRA\u003c\/strong\u003e\u003c\/h3\u003e\n\u003c\/div\u003e\n\u003cdiv\u003e- Te enviamos un kit a tu casa para la recogida de la muestra de ADN (un sencilla muestra de saliva, 2ml) \u003c\/div\u003e\n\u003cdiv\u003e- El envío a tu domicilio, así como el retorno de la muestra al laboratorio, está incluido en el precio (no incluido en las Islas Canarias). Sólo tendrás que seguir las instrucciones que recibirás al activar tu kit.\u003c\/div\u003e\n\u003cdiv\u003e- Desde tu llegada al laboratorio, (aprox. 5 días laborales en Europa), tus resultados estarán listos en 4 semanas.\u003c\/div\u003e\n\u003cdiv\u003e- Podrás acceder a tus resultados en línea, explorar todos los apartados de ADNTRO (salud y farmacogenética incluidos) y a la descarga de ficheros con tu información genética.\u003c\/div\u003e\n\u003ch3\u003e\u003cstrong\u003e\u003c\/strong\u003e\u003c\/h3\u003e\n\u003ch3\u003e\u003cstrong\u003ePREGUNTAS FRECUENTES\u003c\/strong\u003e\u003c\/h3\u003e\n\u003cdiv\u003e\u003cspan style=\"text-decoration: underline;\"\u003e\u003cstrong\u003e¿En qué formatos voy a recibir mis archivos de ADN?\u003c\/strong\u003e\u003c\/span\u003e\u003c\/div\u003e\n\u003cdiv\u003eTe entregaremos varios formatos para que puedas explorar tu ADN:\u003c\/div\u003e\n\u003cdiv\u003e- FASTQ\u003c\/div\u003e\n\u003cdiv\u003e- BAM y BAI\u003c\/div\u003e\n\u003cdiv\u003e- VCF SNP\u003c\/div\u003e\n\u003cdiv\u003e- Informe con validez clínica en PDF\u003c\/div\u003e\n\u003cdiv\u003e- Consulta genética (contratado aparte (*))\u003c\/div\u003e\n\u003cdiv\u003e\u003cbr\u003e\u003c\/div\u003e\n\u003cdiv\u003e\u003cspan style=\"text-decoration: underline;\"\u003e\u003cstrong\u003e¿Qué diferencias hay entre el genotipado (Home Kit) y el Genoma Completo?\u003c\/strong\u003e\u003c\/span\u003e\u003c\/div\u003e\n\u003cdiv\u003eEl genotipado (home kit) analiza aquellas variantes de nuestro genoma que son polimórficas, es decir, que presentan una gran variabilidad entre personas y que son muy frecuentes en general (\u0026gt;1% en la población). Los estudios de asociación genética (GWAS) están fundamentalmente basados en este tipo de análisis y ayudan a determinar  nuestra predisposición a diferentes enfermedades así como a determinar variaciones fenotípicas en los individuos.\u003c\/div\u003e\n\u003cdiv\u003e\u003cbr\u003e\u003c\/div\u003e\n\u003cdiv\u003eLas técnicas de genotipado analizan aproximadamente 700.000 posiciones de nuestro ADN. El análisis del genoma completo (WGS) analiza todo tu ADN (los tres mil millones de pares de bases) y por lo tanto permite la detección de variantes poco frecuentes en la población; estas variantes poco frecuentes suelen tener un elevado impacto en el desarrollo de enfermedades, susceptibilidades a enfermedades y en la  respuesta a tratamientos y es la técnica más empleada en la investigación genética en el mundo.\u003c\/div\u003e\n\u003cdiv\u003e\u003cbr\u003e\u003c\/div\u003e\n\u003cdiv\u003e\n\u003cmeta charset=\"utf-8\"\u003e\n\u003cdiv id=\"elementor-tab-title-1212\" class=\"elementor-tab-title elementor-active\" data-tab=\"2\" role=\"button\" aria-controls=\"elementor-tab-content-1212\" aria-expanded=\"true\" aria-selected=\"true\" tabindex=\"0\"\u003e\u003cspan style=\"text-decoration: underline;\"\u003e\u003cstrong\u003e\u003ca class=\"elementor-toggle-title\" tabindex=\"0\"\u003e¿Cómo funciona y cuánto tiempo tardan los resultados?\u003c\/a\u003e\u003c\/strong\u003e\u003c\/span\u003e\u003c\/div\u003e\n\u003cdiv id=\"elementor-tab-content-1212\" class=\"elementor-tab-content elementor-clearfix elementor-active\" data-tab=\"2\" role=\"region\" aria-labelledby=\"elementor-tab-title-1212\"\u003e\n\u003cp\u003eDesde ADNTRO te enviamos un kit a tu casa para la recogida de la muestra de ADN (un sencilla muestra de saliva, 2ml) – El envío a tu domicilio, así como el retorno de la muestra al laboratorio, está incluido en el precio.\u003c\/p\u003e\n\u003cp\u003eDesde tu llegada al laboratorio, (aprox. 5 días laborales en Europa), tus resultados estarán listos en 4 semanas.\u003c\/p\u003e\n\u003cp\u003ePodrá acceder a tus resultados en línea, explorar todos los apartados de ADNTRO (salud y farmacogenética incluidos) y a la descarga de ficheros con tu información genética.\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cdiv\u003e\n\u003ch3\u003e\n\u003cstrong\u003e¿TIENES DUDAS?\u003c\/strong\u003e\u003cbr\u003e\n\u003c\/h3\u003e\n\u003cp\u003eSi tienes cualquier duda sobre el test, el proceso de análisis o la interpretación de los resultados, nuestro equipo está disponible para ayudarte y orientarte. De forma opcional, puedes contratar una consulta especializada para que un profesional sanitario valore el caso de manera individualizada.\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e","brand":"ADNTRO","offers":[{"title":"Kit de extracción en Domicilio (Extracción con kit en Domicilio del Paciente) [+0,00€] \/ Saliva","offer_id":52708764385546,"sku":"ADNT-0004-10","price":950.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0900\/6661\/6586\/files\/17.jpg?v=1770311145"}],"url":"https:\/\/www.genotica.com\/en\/collections\/secuenciacion-completa-del-genoma-wgs.oembed","provider":"Genotica","version":"1.0","type":"link"}