[카테고리:] FAQ

2026년부터 3B-GENOME(WGS) 검사 샘플을 대상으로 자동 재분석 서비스가 도입됩니다. 본 서비스는 주문 시 재분석을 선택한 사례 중, 결과가 Inconclusive 또는 Negative인 경우에 한해 제공됩니다.

Starting from 2026, automatic reanalysis will be available for 3B-GENOME (WGS) samples. This service is provided only for samples where the reanalysis option was selected at the time of ordering, and is applicable to cases with Inconclusive or Negative results.

CNVs spanning at least three consecutive exons can be detected.

3개 이상의 연속적인 엑손에 걸친 CNV만 검출이 가능합니다.

If your payment link has expired, please contact your 3billion representative or email support@3billion.io and we will send you a new link.For your information, the payment link is valid for two weeks.

This will be used as a reference until final results are available. If an analysis result for a copy number variant is currently unavailable due to sample’s quality control issues, we will first provide a preliminary report.Please note that this report shows preliminary results that are currently suspected and may or may not change in…

Provides additional information on potentially diagnostic variants.Provides a list of variants that are likely to lead to a diagnosis with further testing, such as clinical correlation, segregation testing or functional analysis.Includes VUS variants that may explain the patient’s symptoms but have insufficient evidence of pathogenicity, and pathogenic/likely pathogenic/VUS variants that may explain only part of…

Carrier screening is a test to see if you are a “carrier” of a gene for a specific genetic disorder. A “carrier” is a person who has the gene for a specific genetic disorder, but does not show symptoms of the disorder. This test is mainly used for the following purposes Family planning: couples of…

We can diagnose mtDNA variants in 3B-GENOME and 3B-EXOME from 1st May 2023.We improved the accuracy of the analysis by evenly sequecing the entire mtDNA.

For patient payments, the test will not proceed if payment is not received.