A method of identifying hydrocarbon seeps that are connected to hydrocarbon reservoirs and for identifying in situ conditions of hydrocarbon reservoirs is disclosed. The method comprises, obtaining a sample from an area of interest, such as a sediment sample or water column sample near a hydrocarbon seep; analyzing the sample to detect microbial signatures that are specific to families associated with hydrocarbon reservoirs; and using the signature to determine whether the hydrocarbon seep is connected to a hydrocarbon reservoir and to identify properties of the hydrocarbon reservoir.

A method of identifying hydrocarbon seeps that are connected to hydrocarbon reservoirs and for identifying in situ conditions of hydrocarbon reservoirs is disclosed. The method comprises, obtaining a sample from an area of interest, such as a sediment sample or water column sample near a hydrocarbon seep; analyzing the sample to detect microbial signatures that are specific to families associated with hydrocarbon reservoirs; and using the signature to determine whether the hydrocarbon seep is connected to a hydrocarbon reservoir and to identify properties of the hydrocarbon reservoir.

An oil and gas exploration method based on a microbial gene is provided, where samples are collected from shallow surface layers above a known oil well, a gas well, and a dry well in an exploration area, DNA is extracted and subjected to high-throughput sequencing (HTS), and a pattern map of a microbial community composition in the exploration area is established according to sequencing results; and characteristic microorganisms in surface soil above an oil/gas well in the exploration area are screened out according to the pattern map, then primers are designed according to attribute characters of the characteristic microorganisms, and samples throughout the exploration area are subjected to fluorescence quantitative polymerase chain reaction (PCR) to detect a number of the characteristic microorganisms.

An oil and gas exploration method based on a microbial gene is provided, where samples are collected from shallow surface layers above a known oil well, a gas well, and a dry well in an exploration area, DNA is extracted and subjected to high-throughput sequencing (HTS), and a pattern map of a microbial community composition in the exploration area is established according to sequencing results; and characteristic microorganisms in surface soil above an oil/gas well in the exploration area are screened out according to the pattern map, then primers are designed according to attribute characters of the characteristic microorganisms, and samples throughout the exploration area are subjected to fluorescence quantitative polymerase chain reaction (PCR) to detect a number of the characteristic microorganisms.

A Sampler and process for collecting, growing, inoculating and evaluating microbes in-situ. The Sampler may be loaded with an active or inert media to assist with the collection of microbes. It is closed and lowered to a desired depth. Sampler is opened to initiate sampling. Materials are added to the sampler to stimulate growth or change the environment. To collect and grow in situ microbes, the sampler is left open for a period of time, a trigger closes and seals the sampler capturing contents specific to that location. The sampler is lifted preserving the in-situ conditions from the collection location. The contents of the sampler can be interrogated through sealed ports at the field site or at a remote location. The sampler can also be utilized as a biologic reactor allowing researchers to connect laboratory equipment to analyze, modify, or cultivate the collected sample.

A Sampler and process for collecting, growing, inoculating and evaluating microbes in-situ. The Sampler may be loaded with an active or inert media to assist with the collection of microbes. It is closed and lowered to a desired depth. Sampler is opened to initiate sampling. Materials are added to the sampler to stimulate growth or change the environment. To collect and grow in situ microbes, the sampler is left open for a period of time, a trigger closes and seals the sampler capturing contents specific to that location. The sampler is lifted preserving the in-situ conditions from the collection location. The contents of the sampler can be interrogated through sealed ports at the field site or at a remote location. The sampler can also be utilized as a biologic reactor allowing researchers to connect laboratory equipment to analyze, modify, or cultivate the collected sample.

The present disclosure provides methods of detecting a fusion gene of HNF4G and RSPO2 in a nucleic acid-containing sample, and a primer set, a probe set and a kit for detecting the fusion gene are also provided. Animal models for a human disease positive for the fusion gene are also provided herein. In addition, the present disclosure relates to the methods for assessing and identifying an agent effective on the fusion gene of HNF4G and RSPO2 or a human disease positive for a fusion gene of HNF4G and RSPO2 and thereby treating said disease are also provided.

A method of identifying in situ conditions of a hydrocarbon reservoir is disclosed. The method comprises, obtaining a sample from an area of interest, such as a sediment sample or water column sample near a hydrocarbon seep; analyzing the sample to detect lipid, protein, and/or nucleic acid signatures that are indicative of the Thermotogales order; identifying the relative abundance of the different genera and/or species of the Thermotogales present in the sample to generate a taxonomy signature of the sample; and then using the taxonomy signature to determine conditions, such as temperature, of the hydrocarbon reservoir.

A method of identifying in situ conditions of a hydrocarbon reservoir is disclosed. The method comprises, obtaining a sample from an area of interest, such as a sediment sample or water column sample near a hydrocarbon seep; analyzing the sample to detect lipid, protein, and/or nucleic acid signatures that are indicative of the Thermotogales order; identifying the relative abundance of the different genera and/or species of the Thermotogales present in the sample to generate a taxonomy signature of the sample; and then using the taxonomy signature to determine conditions, such as temperature, of the hydrocarbon reservoir.

A computer supported method, computer system and computer program product for exploring and producing a subsurface heterogeneous hydrocarbon source and generating a predictive production map of an area under investigation, based on microbial prospecting. Microbial data representative of microbial activity attributable to hydrocarbon microseepage and hydrocarbon productivity data of a plurality of geographic locations are retrieved and correlated by the computer in a data correlation algorithm, providing a threshold hydrocarbon productivity quantity and a truncated set of the retrieved microbial data. The set identifies individual types of the microorganisms and corresponding individual weighting factors computed by the data correlation algorithm, for distinguishing prospective hydrocarbon productivity quantities from non-prospective hydrocarbon productivity quantities. An estimated subsurface hydrocarbon productivity quantity for a geographical location of the area under investigation is provided by count weighting retrieved microbial data of this location for microorganisms identified in the truncated set, applying the individual weighting factors.